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Other authors have suggested that using a RME (Rapid Maxillary expansion) or headgrear (EOT) to create sufficient space within the dental arch for the permanent canine tooth will encourage the tooth to erupt (Baccetti et al., 2011). This approach might be less traumatic to a child who may have had no experience of dent... |
<|newrecord|> nctId: NCT06267976 id: REB23-1003 briefTitle: Validation of the ProSomnus® RPMO2 Device overallStatus: NOT_YET_RECRUITING date: 2024-04-10 date: 2024-05-31 date: 2024-06-30 date: 2024-02-20 date: 2024-04-02 name: ProSomnus Sleep Technologies class: INDUSTRY briefSummary: The purpose of the study is to: |
1. Evaluate the SpO2 accuracy of the oximeter component of the ProSomnus RPMO2 Device during non-motion conditions over the range of 70-100% SaO2 by comparison to SaO2 values determined by arterial blood sample specimen analyzed by a CO-oximeter. |
2. Evaluate the pulse rate performance simultaneously collected over the SpO2 range. conditions: Healthy studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: PROSPECTIVE count: 15 type: ESTIMATED name: ProSomnus RPMO2 measure: SpO2 accuracy measure: Pulse rate accuracy sex: ALL minimumAge: 18 Years maxi... |
<|newrecord|> nctId: NCT06267963 id: C4391010 id: 2023-507074-40-00 type: REGISTRY domain: CTIS (EU) briefTitle: A Study to Understand What the Body Does to the Study Medicine Called PF-07220060 When Taken by Healthy Adults overallStatus: ACTIVE_NOT_RECRUITING date: 2024-01-31 date: 2024-04-18 date: 2024-04-18 date: 20... |
The study is seeking for participants who: |
* are males aged 18 to 65 years and are healthy. |
* have Body mass index (BMI) between 17.5 and 30.5 kilograms/meter2 |
* have a total body weight of at least 50 kilograms. |
The study consists of two groups. In group 1, participants will take one amount of PF-07220060 by mouth. In group 2, participants will take one amount by mouth and one amount as an injection through a vein at the study clinic. |
In group 1, participants will stay at the clinic site for up to 15 days. In group 2, the duration of participants' stay depends on the results of group 1. |
During their stays, participants will have their blood, urine, and feces collected by the study doctors several times. We will measure the level of PF-07220060 in participants' blood, urine, and feces samples. This will help to know how much the study medicine is getting taken up by the body. At the end of the study, p... |
<|newrecord|> nctId: NCT06267950 id: PILUO-INFANT briefTitle: Effect of Oral Feeding in Infants With Pierre Robin Syndrome overallStatus: RECRUITING date: 2024-02-29 date: 2024-10 date: 2024-10 date: 2024-02-20 date: 2024-03-06 name: Zeng Changhao class: OTHER briefSummary: This was a randomized controlled study. The i... |
<|newrecord|> nctId: NCT06267937 id: 101 briefTitle: Hip Fractures in Chile: Implications for Public Health Policy and Healthcare Delivery overallStatus: COMPLETED date: 2023-03-10 date: 2023-03-10 date: 2024-01-30 date: 2024-02-20 date: 2024-02-20 name: University of Chile class: OTHER name: Instituto Sistemas Complej... |
<|newrecord|> nctId: NCT06267924 id: Olith10703 briefTitle: SENSE-VM: Safety and Effectiveness of a Novel Medical Device for Symptom Ease in Vestibular Migraines overallStatus: ENROLLING_BY_INVITATION date: 2024-02-28 date: 2024-08-31 date: 2024-09-30 date: 2024-02-20 date: 2024-03-19 name: Otolith Labs class: INDUSTRY... |
Participants will be: |
* Enrolled up to 50 days; enrollment, 14 days in Baseline Phase (no device), 7 days in Transition Phase, 28 days in Treatment Phase (study device) |
* Randomized and stratified into groups based on the referring clinic to be assigned one study device |
* Asked to use the study device as instructed by the study coordinator |
* Asked to submit daily diaries reporting their symptoms and use of device, and to participate in tele-health visits with study coordinators |
* Asked to provide their vertigo diagnosis from their physician |
* Compensated for their participation |
Researchers will compare the randomized groups to determine which group responds better to which device. conditions: Vestibular Migraine conditions: Migraine Associated Vertigo studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: The proposed clinical tri... |
<|newrecord|> nctId: NCT06267911 id: 202223-10 id: 160/U/2022 type: OTHER_GRANT domain: Fundació La Marató de TV3 briefTitle: Rehabilitation Gaming System for Intensive Care Units acronym: RGS-ICU overallStatus: NOT_YET_RECRUITING date: 2024-05 date: 2026-04 date: 2026-04 date: 2024-02-20 date: 2024-04-23 name: Univers... |
This trial aims to evaluate the efficacy of an innovative neuropsychological e-health intervention for early cognitive stimulation and psychological support of people in critical care, i.e. the Rehabilitation Gaming System for Intensive Care Units (RGS-ICU) intervention, in improving comfort during ICU admission and co... |
The investigadors hypothesize that the cognitive stimulation and psychological support protocols of the RGS-ICU intervention, applied as an adjunct to standard ICU care, in addition to being safe for people in critical care units, will improve comfort during ICU admission and cognitive and mental health outcomes after ... |
The findings derived from this trial may contribute to establish a novel and superior paradigm of human-centered ICU care to improve the comfort of people admitted to the ICU. This achievement could also have a relevant impact on medical and economic costs during ICU admission, and on functionality and health-related q... |
The RGS-ICU intervention has been designed at Corporacion Parc Taulí with the collaboration of the University of the Balearic Islands and has been developed by Eodyne Systems S.L., a company dedicated to the development of science-based technological solutions for intervention, monitoring, diagnosis, and prognosis in s... |
<|newrecord|> nctId: NCT06267898 id: EBMT- 842205547 briefTitle: Non Interventional Study on Iron Toxicity After First Allo-transplant in MDS/CMML overallStatus: COMPLETED date: 2009-11-01 date: 2015-01-29 date: 2015-05-21 date: 2024-02-20 date: 2024-02-20 name: European Society for Blood and Marrow Transplantation cla... |
Toxic effects of iron may play an important role in the complications associated with HSCT. Iron chelation therapy may reduce the acute and chronic treatment-related toxicity by removing excess of iron, iron radicals and reactive oxygen species (ROS). |
There is little information about the efficacy and safety of iron chelation in MDS patients. This audit wants to evaluate the effect of iron toxicity on treatment-related mortality in untreated, adult MDS or CMML patients during and after treatment with myeloablative conditioning (MAC) and reduced intensity conditionin... |
<|newrecord|> nctId: NCT06267885 id: Children NOF fracture fixation briefTitle: Fixation of Fracture Neck of Femur in Children overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2026-02 date: 2026-03 date: 2024-02-20 date: 2024-02-20 name: Assiut University class: OTHER briefSummary: Find the best way for fixation o... |
<|newrecord|> nctId: NCT06267872 id: HVTN 309 briefTitle: A Clinical Trial in Adult Participants Without HIV and in Overall Good Health to Evaluate the Safety and Immunogenicity of CD4BS CH505M5 Pr-NP1 Followed by CH505 TF chTrimer Boost Both Adjuvanted With Either Lipid Nanoparticles (LNPs) or 3M-052-AF + Alum overall... |
About 42 people will take part in the HVTN 309 clinical trial. This clinical trial will take place at multiple sites in the US and South Africa and the clinical trial is divided into 3 parts: Part A, Part B and Part C. About 3 people will participate in Part A of this study. After results from Part A are reviewed, it w... |
<|newrecord|> nctId: NCT06267859 id: No. 2 of 2023/11/7 briefTitle: Development of Methods for Effective Treatment and Improvement of Common Somatic Diseases in Children overallStatus: RECRUITING date: 2023-11-08 date: 2033-12-30 date: 2034-01-30 date: 2024-02-20 date: 2024-02-28 name: Tashkent Pediatric Medical Instit... |
The main questions it aims to answer: |
* Analysis of common congenital diseases among children; |
* Analysis of commonly diagnosed bronchopulmonary and cardiovascular diseases among children; |
* Based on the results of the primary research, common diseases among children will be identified; |
* Analysis of existing treatment methods and their effectiveness; |
* Development of modern methods of treatment and rehabilitation of children. conditions: Respiratory Diseases conditions: Congenital Heart Defects studyType: INTERVENTIONAL phases: EARLY_PHASE1 allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: identification of children from the group of ... |
<|newrecord|> nctId: NCT06267846 id: NBI-1070770-MDD2029 briefTitle: A Study to Evaluate the Efficacy and Safety of NBI-1070770 in Adults With Major Depressive Disorder overallStatus: RECRUITING date: 2024-03-20 date: 2025-09 date: 2025-12 date: 2024-02-20 date: 2024-04-12 name: Neurocrine Biosciences class: INDUSTRY b... |
<|newrecord|> nctId: NCT06267833 id: MSKUSBFFTR01 briefTitle: The Effect of Trunk and Upper Extremity Exercises Added to the Otago Exercise Program acronym: Otago Exercise overallStatus: NOT_YET_RECRUITING date: 2024-09-01 date: 2026-01-01 date: 2026-06-01 date: 2024-02-20 date: 2024-02-20 name: Muğla Sıtkı Koçman Univ... |
<|newrecord|> nctId: NCT06267820 id: 2010 briefTitle: Postoperative Pain Control by Adding Ketorolac to Bupivacaine in Transversus Abdominis Plane Block in Children overallStatus: COMPLETED date: 2023-06-01 date: 2023-12-01 date: 2023-12-10 date: 2024-02-20 date: 2024-02-20 name: Sohag University class: OTHER briefSumm... |
Ketorolac has analgesic effect comparable to morphine. Children were arranged randomly into two equal groups, forty-five children in each. |
Group (K) (n= 45): received ultrasound guided TAP block with bupivacaine 0.25% (0.5 ml/kg) and ketorolac (0.5 mg/kg). |
Group (T) (n =45): received ultrasound guided TAP block with bupivacaine 0.25% (0.5 ml/kg) conditions: Postoperative Pain, Acute studyType: INTERVENTIONAL phases: PHASE2 allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: HEALTH_SERVICES_RESEARCH masking: QUADRUPLE whoMasked: PARTICIPANT whoMasked: CARE_... |
<|newrecord|> nctId: NCT06267807 id: 114369 id: NL84520.091.23 type: OTHER domain: Protocol ID METC briefTitle: Lymphatic Phenotype in Noonan Syndrome Spectrum Disorders acronym: LENS overallStatus: RECRUITING date: 2024-03-27 date: 2025-03-13 date: 2025-06-01 date: 2024-02-20 date: 2024-02-20 name: Radboud University ... |
<|newrecord|> nctId: NCT06267794 id: ODISEA Study briefTitle: Prolonged Release Pirfenidone Versus Placebo in Compensated Cirrhosis. acronym: ODISEA overallStatus: COMPLETED date: 2015-06-26 date: 2021-12-30 date: 2023-03-24 date: 2024-02-20 date: 2024-02-20 name: Jorge L Poo class: OTHER briefSummary: This will be a m... |
Methods to assign treatment: |
Before assigning numbers to subjects, the researcher must confirm that the inclusion criteria have been met, that none of the exclusion criteria apply, that written and signed informed consent has been obtained, that the evaluations of the scrutiny (of admission) and that the required laboratory results are available a... |
The person responsible for the medication at the research site will contact the Randomization center, where the treatment will be assigned to the patient. whoMasked: PARTICIPANT whoMasked: CARE_PROVIDER whoMasked: INVESTIGATOR count: 180 type: ACTUAL name: Pirfenidone 1200 mg name: Pirfenidone 1800 mg name: Placebo mea... |
<|newrecord|> nctId: NCT06267781 id: TRANSPLANT-PRO briefTitle: RRMS: Disease PROgression and Myeloid Profiling After Bone Marrow TRANSPLANTation and Second Line Therapies acronym: TRANSPLANTPRO overallStatus: RECRUITING date: 2022-09-02 date: 2027-09-02 date: 2027-09-02 date: 2024-02-20 date: 2024-02-20 name: IRCCS Sa... |
<|newrecord|> nctId: NCT06267768 id: REC Reference No.:HE-OT2023/13 id: Proj.Ref.No.: 2023/3007-R7052 type: OTHER_GRANT domain: Research Donation Fund, Hong Kong Metropolitan University briefTitle: The Effects of Inspiratory Pressures on Diaphragmatic Contraction in People After Stroke overallStatus: NOT_YET_RECRUITING... |
<|newrecord|> nctId: NCT06267755 id: P.T.REC/012/004884 briefTitle: Efficacy of Extracorporeal Shockwave Therapy on Ultrasonography Changes of Upper Trapezius Myofascial Trigger Points in Patients With Non Specific Neck Pain acronym: MTP overallStatus: NOT_YET_RECRUITING date: 2024-02-20 date: 2024-08-30 date: 2024-08-... |
<|newrecord|> nctId: NCT06267742 id: CHN097 briefTitle: Clinical Trial to Evaluate MDW for Early Detection of Sepsis overallStatus: RECRUITING date: 2022-06-23 date: 2024-03-31 date: 2024-09-30 date: 2024-02-20 date: 2024-02-28 name: Beckman Coulter, Inc. class: INDUSTRY name: Peking Union Medical College Hospital name... |
<|newrecord|> nctId: NCT06267729 id: D9660C00001 briefTitle: Study of AZD0754 in Participants With Metastatic Prostate Cancer acronym: APOLLO overallStatus: RECRUITING date: 2024-03-12 date: 2027-05-24 date: 2027-05-24 date: 2024-02-20 date: 2024-04-29 name: AstraZeneca class: INDUSTRY briefSummary: The purpose of this... |
<|newrecord|> nctId: NCT06267716 id: 274-2023 briefTitle: Pericapsular Nerve Block and Iliopsoas Fascial Plane Block in Hip Surgery overallStatus: RECRUITING date: 2024-02-23 date: 2024-07-30 date: 2024-08-30 date: 2024-02-20 date: 2024-02-28 name: Haseki Training and Research Hospital class: OTHER briefSummary: This p... |
The main questions it aims to answer are the effectivity of postoperative pain management the preservation of motor movement. |
Participants will receive standardized general anesthesia and postoperative PENG or IPB in either Group. |
Researchers will compare the total amount of rescue analgesia and numeric rating scale with accompanying evaluating motor function at the same time intervals within 24 hour. conditions: Hip Fractures conditions: Peripheral Nerve Block studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALL... |
<|newrecord|> nctId: NCT06267703 id: 2023-01939_VR briefTitle: Multi-omics Analyses on Etiology and Early Detection of Stomach Cancer Precursor Lesions overallStatus: ACTIVE_NOT_RECRUITING date: 2024-01-01 date: 2026-12-31 date: 2026-12-31 date: 2024-02-20 date: 2024-02-21 name: Karolinska Institutet class: OTHER brief... |
<|newrecord|> nctId: NCT06267690 id: SYSUFAH2021025 briefTitle: A CT-based Radiomics Model to Predict Survival-graded Fibrosis in PDAC overallStatus: COMPLETED date: 2021-01-13 date: 2023-08-31 date: 2023-08-31 date: 2024-02-20 date: 2024-02-20 name: First Affiliated Hospital, Sun Yat-Sen University class: OTHER briefS... |
<|newrecord|> nctId: NCT06267677 id: 2007/3928 briefTitle: Efficacy of Liquid Versus Powder Protein Supplementation to Optimize Protein Intake After Bariatric Surgery overallStatus: COMPLETED date: 2008-01-02 date: 2008-04-18 date: 2009-03-06 date: 2024-02-20 date: 2024-02-20 name: Hospital Clinic of Barcelona class: O... |
Participants will be evaluated at the beginning, at 1 month and at the end of the study (2m) and the following determinations will be made: |
* Analytical determination |
* Nitrogen balance by determining urea N2 in 24-hour urine |
* Anthropometric determinations |
* Body composition determined by impedanciometry |
* Resting energy expenditure and nutrient oxidation measured by indirect calorimetry. |
* Energy, protein and hydration intake. |
* Gastrointestinal tolerance through self-registration of symptoms. Researchers will compare the effect of a complete hypocaloric liquid formula group with the usual progressive diet group to see if they achieve the protein intake goal established for patients after obesity surgery, preservation of nutritional status a... |
<|newrecord|> nctId: NCT06267664 id: PI-GR-23-3263 briefTitle: Real-world Effectiveness and Tolerability of Triptans-Ditans-Gepants (TRIDIGEP) acronym: TRIDIGEP overallStatus: RECRUITING date: 2023-12-04 date: 2024-09-30 date: 2024-12-01 date: 2024-02-20 date: 2024-02-21 name: Hospital Clínico Universitario de Valladol... |
The TRIDIGEP study will be an open-label, multiple attack, prospective cohort study. |
This study aims to describe 1) the effectiveness of the acute treatments of migraine attacks in routine clinical practice, 2) the tolerability of the drugs, and 3) to explore potential response and tolerability predictors. |
The endpoints recommended by the International Headache Society will be employed, including: 1) Pain freedom; 2) Absence of the most bothersome symptom; 3) Sustained pain freedom; 4) Total freedom from migraine; 5) Headache relief; 6) Duration of attacks; 7) Time lost due to an attack; 8) Need of rescue medication. The... |
<|newrecord|> nctId: NCT06267651 id: Steroid in ulcerative colitis briefTitle: Value Of ACE Index (Albumin, CRP And Endoscopy) In Predicting Intra Venous Steroid Response In Acute Severe Ulcerative Colitis In Assiut University Hospitals overallStatus: NOT_YET_RECRUITING date: 2025-01 date: 2026-06 date: 2027-01 date: 2... |
2. identify on admission a high-risk population who may beneft from earlier second line medical treatment or surgical intervention. ( steroid non responder groups ) conditions: Early Detection of Complication of Ulcerative Colitis studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: PROSPECTIVE count: 9... |
<|newrecord|> nctId: NCT06267638 id: Chomthong hospital, Thailand briefTitle: Comparison of Postoperative Pain Score Between Perioperative Intravenous Ketamine and Placebo in Patients Undergoing Unilateral Total Knee Arthroplasty Under General Anesthesia overallStatus: RECRUITING date: 2024-01-22 date: 2025-12-31 date:... |
* Can perioperative intravenous ketamine reduce postoperative pain score during rest and movement at 0, 2, 4, 8, 12, 18, 24 hours better than no administration of Ketamine in patients undergoing Unilateral total knee arthroplasty under general anesthesia? |
* Can perioperative intravenous ketamine reduce morphine consumption in postoperative 24 hours, length of hospital stay, first time to receive opioid and side effect or complication from ketamine and opioid better than no administration of Ketamine in patients undergoing Unilateral total knee arthroplasty under general... |
<|newrecord|> nctId: NCT06267625 id: Elderly Individuals briefTitle: Physical Impairments in Elderly Individuals overallStatus: NOT_YET_RECRUITING date: 2024-03-15 date: 2026-03-15 date: 2026-12-15 date: 2024-02-20 date: 2024-02-20 name: Izmir Democracy University class: OTHER briefSummary: There are no studies in the ... |
<|newrecord|> nctId: NCT06267612 id: KY20231109-11 briefTitle: Corheart 6 LVAS Long-term Follow-up Study overallStatus: NOT_YET_RECRUITING date: 2024-02-10 date: 2030-06-30 date: 2030-06-30 date: 2024-02-20 date: 2024-02-20 name: Nanjing First Hospital, Nanjing Medical University class: OTHER briefSummary: The purpose ... |
The study will be a single-arm, prospective, single-center, non-blinded, and non-randomized study with a follow-up duration of five years. conditions: Heart Failure studyType: INTERVENTIONAL phases: NA allocation: NA interventionModel: SINGLE_GROUP primaryPurpose: TREATMENT masking: NONE count: 30 type: ESTIMATED name:... |
<|newrecord|> nctId: NCT06267599 id: ACAR-Style Bladder Suture briefTitle: Bladder Suture in Uterus-Sparing Surgery and Hysterectomy for Placenta Percreta overallStatus: COMPLETED date: 2023-09-01 date: 2023-12-01 date: 2024-01-01 date: 2024-02-20 date: 2024-02-20 name: Necmettin Erbakan University class: OTHER briefSu... |
<|newrecord|> nctId: NCT06267586 id: PN23.007 briefTitle: Effects of PeptiSleep in Healthy Males and Females With Mild to Moderate Sleep Impairment overallStatus: RECRUITING date: 2024-04-08 date: 2024-12-30 date: 2025-02-20 date: 2024-02-20 date: 2024-04-24 name: Nuritas Ltd class: INDUSTRY name: RDC Clinical Pty Ltd ... |
<|newrecord|> nctId: NCT06267573 id: Kerolos protocol briefTitle: Thoracoabdominal Aortic Aneurysms overallStatus: NOT_YET_RECRUITING date: 2024-09 date: 2025-09-15 date: 2026-09-10 date: 2024-02-20 date: 2024-02-20 name: Assiut University class: OTHER briefSummary: Evaluation of the effectiveness of the different moda... |
<|newrecord|> nctId: NCT06267560 id: CTQJ230A12303 briefTitle: Lp(a) Lowering Study of Pelacarsen (TQJ230) in US Black/African American and Hispanic Participants With Elevated Lp(a) and Established ASCVD overallStatus: NOT_YET_RECRUITING date: 2024-05-27 date: 2027-06-21 date: 2027-06-21 date: 2024-02-20 date: 2024-02-... |
<|newrecord|> nctId: NCT06267547 id: 2023P003522 briefTitle: Healthy Activities Improve Lives (HAIL) acronym: HAIL overallStatus: RECRUITING date: 2024-04-23 date: 2026-12-01 date: 2027-02-01 date: 2024-02-20 date: 2024-04-29 name: Massachusetts General Hospital class: OTHER name: National Institute on Aging (NIA) brie... |
<|newrecord|> nctId: NCT06267534 id: YCH briefTitle: Mindfulness-based Mobile Applications Program overallStatus: COMPLETED date: 2022-09-09 date: 2022-09-22 date: 2022-09-22 date: 2024-02-20 date: 2024-02-20 name: Yu-Chien Huang class: OTHER briefSummary: The goal of this type of study: quasi-experimental clinical tri... |
1. To explore the effect of mindfulness-based mobile device-assisted program on care stress of emergency nurses caring for COVID-19 patients. |
2. To explore the impact of mindfulness-based mobile device-assisted programs on the psychological distress of emergency nurses caring for COVID-19 patients. |
3. To explore the impact of a mindfulness-based mobile device-assisted program on compassion fatigue in emergency nurses caring for COVID-19 patients. |
Participants will Mindfulness-based mobile device is provided to experimental group as assistance for 2 weeks. In the contrary, no intervention measure was assigned in the control group. Scale exam was performed before and after the program in both groups at the same time. conditions: COVID-19 conditions: Cell Phone Us... |
<|newrecord|> nctId: NCT06267521 id: 2023-1473 id: Protocol Version 2/8/2024 type: OTHER domain: UW Madison id: L&S/PSYCHOLOGY/PSYCHOLOGY type: OTHER domain: UW Madison id: A487400 type: OTHER domain: UW Madison id: AWD00000302 type: OTHER_GRANT domain: US Department of Defense DARPA briefTitle: The STRENGTHEN Study ov... |
<|newrecord|> nctId: NCT06267508 id: LMU-IMPH-LIFE2Scale briefTitle: Increasing Neonatal HIV Test and Treat to Maximize the Long-Term Impact on Infant Health and Novel Infant Antiretroviral Treatment acronym: LIFE2Scale overallStatus: NOT_YET_RECRUITING date: 2024-03 date: 2025-12 date: 2025-12 date: 2024-02-20 date: 2... |
<|newrecord|> nctId: NCT06267495 id: EOCXLFE briefTitle: Epithelium-on Cross-linking Versus Observation of Fellow Eyes of Patients With Unilateral Clinically Evident Keratoconus overallStatus: COMPLETED date: 2017-01-01 date: 2024-01-31 date: 2024-01-31 date: 2024-02-20 date: 2024-02-20 name: Assiut University class: O... |
The aim of the current study is to investigate the effectiveness and safety of epithelium-on accelerated CXL to stabilize the eye with no clinical signs of KC, in young patients with unilateral clinically evident KC, compared with standard care and follow-up only. conditions: Keratoconus studyType: OBSERVATIONAL observ... |
<|newrecord|> nctId: NCT06267482 id: 122311 briefTitle: Using ROSA for Challenging The TKA Standard of Care overallStatus: RECRUITING date: 2024-04-16 date: 2025-04 date: 2025-06 date: 2024-02-20 date: 2024-04-18 name: Lawson Health Research Institute class: OTHER name: Zimmer Biomet briefSummary: This is a prospective... |
1. Standard of care medial parapetallar approach (Control) |
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