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<|newrecord|> nctId: NCT06318091 id: MS.21.09.1640 briefTitle: Nanofat Versus Platelet Poor Plasma Gel for Infraorbital Rejuvenation overallStatus: COMPLETED date: 2021-06-01 date: 2023-06-01 date: 2023-06-01 date: 2024-03-19 date: 2024-03-19 name: Mansoura University class: OTHER briefSummary: this study was conducted... |
<|newrecord|> nctId: NCT06318078 id: UG2024001 briefTitle: Buikwe Electronic Community Health Information System Impact Study overallStatus: RECRUITING date: 2023-12-01 date: 2024-04 date: 2024-07 date: 2024-03-19 date: 2024-03-19 name: Malaria Consortium class: OTHER briefSummary: The purpose of the study is to invest... |
<|newrecord|> nctId: NCT06318065 id: B-ER111-370 briefTitle: Surgical Resection Outcomes in Patients With Brain Metastasis overallStatus: RECRUITING date: 2010-01-01 date: 2024-06-01 date: 2024-09-01 date: 2024-03-19 date: 2024-03-22 name: National Cheng-Kung University Hospital class: OTHER briefSummary: While many st... |
<|newrecord|> nctId: NCT06318052 id: LUM-ABU-CO2-FemTouch-19-01 briefTitle: The Effect Of Fractional CO2 Laser Therapy On Cancer Survivors With Genitourinary Syndrome Of Menopause (GSM) overallStatus: RECRUITING date: 2019-11-01 date: 2024-11 date: 2024-11 date: 2024-03-19 date: 2024-03-20 name: Lumenis Be Ltd. class: ... |
<|newrecord|> nctId: NCT06318039 id: IRB2022-06554-01 briefTitle: Operation ACL: Rehabilitation After Anterior Cruciate Ligament Reconstruction overallStatus: NOT_YET_RECRUITING date: 2024-10-01 date: 2027-03-01 date: 2027-10-01 date: 2024-03-19 date: 2024-04-08 name: Linnaeus University class: OTHER briefSummary: Scie... |
Overall Purpose: |
Regarding rehabilitation after anterior cruciate ligament reconstruction (ACLR), there is a knowledge gap - a lack of evidence. Important questions such as how rehabilitation should be structured, what it should include, and how it should be evaluated are currently not clear. Therefore, the investigators plan to conduc... |
Moreover, detailed information on how/under what circumstances the ACL injury occurred is not satisfactorily described in the literature. Therefore, the investigators are planning a new survey that can identify, explain, and prevent the risk factors causing a person to suffer from an anterior cruciate ligament injury. |
Specific Objectives: |
How should guidelines for rehabilitation after ACLR be structured, what should they include, and how should they be evaluated to best restore knee function in the patient? Can a detailed and comprehensive survey identify, explain, and prevent the risk factors causing a person to suffer from an ACL injury? conditions: A... |
<|newrecord|> nctId: NCT06318026 id: R01AA031231 type: NIH link: https://reporter.nih.gov/quickSearch/R01AA031231 id: R01AA031231 type: NIH link: https://reporter.nih.gov/quickSearch/R01AA031231 briefTitle: Systematic Implementation of Patient-centered Care for Alcohol Use Trial: Beyond Referral to Treatment overallSta... |
<|newrecord|> nctId: NCT06318013 id: 2022-KAEK-15427-04-204-2022101 briefTitle: Perineural and Systemic Dexamethasone Use in Dental Surgeries in Terms of Anesthesia Duration and Postop Complaints overallStatus: RECRUITING date: 2024-03-27 date: 2024-04-15 date: 2024-07-01 date: 2024-03-19 date: 2024-03-29 name: Karaman... |
<|newrecord|> nctId: NCT06318000 id: SN4/20/22 briefTitle: Physical Activity and Sports for People With Visual Impairments overallStatus: COMPLETED date: 2020-03-01 date: 2022-12-31 date: 2022-12-31 date: 2024-03-19 date: 2024-03-20 name: Józef Piłsudski University of Physical Education class: OTHER briefSummary: Purpo... |
<|newrecord|> nctId: NCT06317987 id: 2068557 id: P50DA054072 type: NIH link: https://reporter.nih.gov/quickSearch/P50DA054072 briefTitle: Addressing Barriers to Care for Substance Use Disorder Pilot Study acronym: ABCSUD Pilot overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2025-04-02 date: 2025-04-02 date: 20... |
This study will be conducted in a mental health treatment access center within the Washington region of Kaiser Permanente. As part of usual care, patients contact the mental health access center and speak to a "care coordinator" to obtain contact information for potential venues to obtain treatment for substance use di... |
The experimental intervention, Care Navigation, will be evaluated for its potential to increase the utilization of substance use disorder treatment among patients who contact the mental health treatment access center. The investigators note that Care Navigation will be delivered by study "care navigators", who are dist... |
<|newrecord|> nctId: NCT06317974 id: 2022/210 briefTitle: The Effect of Breastfeeding Education on Breast Milk Perception and Self-Efficacy in the Pregnancy Health Belief Model overallStatus: COMPLETED date: 2022-06-30 date: 2022-12-31 date: 2023-02-15 date: 2024-03-19 date: 2024-03-19 name: Istanbul University - Cerra... |
<|newrecord|> nctId: NCT06317961 id: INT200-22 briefTitle: Pilot Study on the Use of iENTER, iCONSENT and iPARTICIPATE E-tools overallStatus: RECRUITING date: 2023-04-05 date: 2025-01-31 date: 2025-01-31 date: 2024-03-19 date: 2024-03-19 name: Fondazione IRCCS Istituto Nazionale dei Tumori, Milano class: OTHER name: Va... |
<|newrecord|> nctId: NCT06317948 id: IG23150 briefTitle: Improving the Quality of Radiotherapy by Multi-Institution Knowledge-Based Planning Optimization Models (Acronym: MIKAPOCo, Multi-Institutional Knowledge-based Approach in Plan Optimization for the Community) acronym: MIKAPOCo overallStatus: ENROLLING_BY_INVITATI... |
Quantifying Inter-institute variability of RT planning and building libraries of interchangeable and validated multi-Institutional KB plan prediction models is expected to impact on the quality of planning at the national level. The project has the potential of facilitating the introduction of AI approaches in plan opt... |
<|newrecord|> nctId: NCT06317935 id: HU-ERG-BK-01 briefTitle: The Effect of Virtual Reality Application on Independence and Hand Functions in Daily Life in Children With CP overallStatus: NOT_YET_RECRUITING date: 2024-04-23 date: 2024-06-29 date: 2024-10-29 date: 2024-03-19 date: 2024-03-19 name: Hacettepe University c... |
The research is a randomized controlled, cross-over study. The sample group of the research is children diagnosed with hemiplegic cerebral palsy and families who are receiving inpatient treatment in the pediatric service of Ankara City Hospital Physical Therapy and Rehabilitation Hospital. |
Two groups, intervention (A) and control (B), will be created from the target research group using the randomization method. |
The upper extremity functionality of both research groups before the intervention will be evaluated with the 'Motor Activity Diary for Children' scale and the perceived independence level with the 'Children's Hand Use Experience' scale. |
After the initial evaluation is completed, group A, represented as the intervention group, will receive ArmeoSenso virtual reality intervention in the upper extremity hand function laboratory for 3 weeks, 5 days a week, each session for 30 minutes, in addition to traditional occupational therapy and physiotherapy rehab... |
Measurement tools will be repeated at the beginning of the intervention, at the end of the 3rd week, and at the end of the intervention. conditions: Hemiplegic Cerebral Palsy studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: CROSSOVER interventionModelDescription: Two groups, intervention (... |
Intervention group (A) will receive virtual reality application for 30 minutes, 5 days a week for 3 weeks, in addition to traditional occupational therapy and physiotherapy approaches for the first 3 weeks, and will receive only traditional treatments between 3-6 weeks. |
The control group (B) will receive only traditional occupational therapy and physiotherapy approaches for the first 3 weeks, and between 3-6 weeks, they will receive virtual reality application in addition to traditional approaches for 30 minutes, 5 days a week for 3 weeks. primaryPurpose: SUPPORTIVE_CARE masking: DOUB... |
<|newrecord|> nctId: NCT06317922 id: DRYEYE-IVT Project briefTitle: Evaluation of Dry Eye Disease's Signs in Patients Who Were Administered Intravitreal Anti-VEGF Injections acronym: DRYEYE-IVT overallStatus: RECRUITING date: 2024-02-05 date: 2025-05-12 date: 2025-05-12 date: 2024-03-19 date: 2024-03-20 name: Francesco... |
The main questions it aims to answer are: |
* can ocular instillation of Thealoz Duo solution, 1 week before intravitreal injection, in a fixed dose regimen, prevent ocular surface changes and dry-eye signs? |
* can ocular instillation of Thealoz Duo solution, up 3 months after intravitreal injections, in a fixed dose regimen, reduce ocular surface changes, and dry-eye signs with improvement of quality of life and quality of vision? |
Each participant will be randomized into each of two arms: |
1. TREATMENT ARM: patients who will receive the instillation of Thealoz Duo, 10 ml, 1 drop, 4 times/day; |
2. CONTROL ARM: patients who will receive the instillation of saline solution (Hydrabak), 10 ml, 1 drop, 4 times /day; |
The decision of inclusion of a control group should minimize the risk of breaking the blinding condition by affecting the consistency and reliability of the outcome's achievement. |
In any case, the instillation of saline solution should not alter the ocular surface. conditions: Dry Eye Syndromes studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: The participants will be randomized in two arms (treatment arm and control arm) in a r... |
1. MASKED TEAM: Sub-investigators and study coordinators delegated to perform the following tasks: |
* dispensation to the patient the Investigational medical device (Thealoz Duo) or saline solution (Hydrabak containing Sodium Chloride 0,9 g, Sodium Dihydrogen Phosphate Dihydrate, Disodium Hydrogen Phosphate Dodecahydrate); |
* accountability of Investigational medical device and saline solution; |
* verify the compliance and therapeutic adherence of the patient; |
* discussion with the patient regarding the respect of the masked condition of the study; |
2. UNMASKED TEAMS: |
* informed consent process; |
* to perform the follow-up visit and assessments provided to test the ocular surface. whoMasked: CARE_PROVIDER whoMasked: INVESTIGATOR whoMasked: OUTCOMES_ASSESSOR count: 60 type: ESTIMATED name: Thealoz Duo; name: sham (Hydrabak) measure: Administration of Ocular Surface Disease Index (OSDI) to the patient measure:... |
<|newrecord|> nctId: NCT06317909 id: 23-03 DONNER-2 briefTitle: Development of a Novel Non-invasive Inflammometry Following Allergen Challenge in Patients With Mild Allergic Asthma overallStatus: RECRUITING date: 2024-06-01 date: 2025-09 date: 2025-09 date: 2024-03-19 date: 2024-03-19 name: Fraunhofer-Institute of Toxi... |
The investigator wants to further profile and develop the allergen challenge model by investigating the utility of various non-invasive monitoring methods. The hypothesis of the project is that local inflammatory changes in the lung induced by allergen can be captured by gas-enhanced magnetic resonance imaging (MRI) an... |
The validation of cellular outcome measures and non-invasive inflammometry can be used in future clinical trials for proof of concept of novel anti-inflammatory medications. |
Participants will undergo |
* methacholine challenge |
* 2 inhaled allergen challenges |
* 2 MRI with hyperpolarized xenon and gadolinium based contrast agent |
* 2 bronchoscopies with bronchoalveolar lavage (BAL) |
* segmental allergen challenge during the first bronchoscopy |
* spirometry |
* skin prick test and skin prick dilution tests |
* measurement of particles in exhaled air |
* nasal filter |
* nasal lavage |
* sputum induction |
* peak flow meter tests |
* exhaled NO (nictric oxide) |
* blood sampling (in total approx. 190 ml) conditions: Mild Allergic Asthma studyType: INTERVENTIONAL phases: NA allocation: NA interventionModel: SINGLE_GROUP primaryPurpose: OTHER masking: NONE count: 15 type: ESTIMATED name: allergen challenge measure: Exploratory (1. priority) Changes in soluble mediators [i.e. IL-... |
<|newrecord|> nctId: NCT06317896 id: 2024-KY-048-01 briefTitle: Value of Dynamic Monitoring of Early Recurrence of Hepatocellular Carcinoma After Radical Resection Based on CTCS overallStatus: NOT_YET_RECRUITING date: 2024-04-01 date: 2026-12-31 date: 2026-12-31 date: 2024-03-19 date: 2024-03-19 name: Zhujiang Hospital... |
<|newrecord|> nctId: NCT06317883 id: CORALS briefTitle: Childhood Obesity Risk Assessment Longitudinal Study acronym: CORALS overallStatus: ACTIVE_NOT_RECRUITING date: 2019-05-27 date: 2032-07-14 date: 2032-07-14 date: 2024-03-19 date: 2024-03-19 name: Consorcio Centro de Investigación Biomédica en Red (CIBER) class: O... |
From childhood, obesity is associated with an increased risk of diseases such as insulin resistance, type 2 diabetes, hypertension, metabolic syndrome, musculoskeletal problems, sleep disorders and mental health problems. Obesity is a complex, multi-causal problem involving individual risk factors such as behavior and ... |
The aim of the present study is to identify risk factors for childhood obesity through long-term longitudinal follow-up. conditions: Child Obesity studyType: OBSERVATIONAL observationalModel: COHORT timePerspective: PROSPECTIVE count: 1508 type: ACTUAL measure: Assessment of dietary intake and habits measure: Assessmen... |
<|newrecord|> nctId: NCT06317870 id: CHUV_PENGIT briefTitle: Pericapsular Nerve Block Versus Intrathecal Morphine for Analgesia After Primary Hip Arthroplasty acronym: PENGIT overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2027-01-01 date: 2027-05-01 date: 2024-03-19 date: 2024-03-19 name: Centre Hospitalier U... |
Participants will be randomised into two groups. Patients assigned to the PENG group will receive spinal anaesthesia with local anaesthetic (isobaric bupivacaine) alone and a PENG block. Patients assigned to the intrathecal morphine (ITM) group will receive spinal anaesthesia with a mixture of local anaesthetic (isobar... |
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