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Evaluation is based on a parallel group study design, with half of the participants receiving care as usual and half of the participants receiving care as usual along with the Playful Learning in Infancy Program. conditions: Parent-Child Relations conditions: Infant Development studyType: INTERVENTIONAL phases: NA allo... |
<|newrecord|> nctId: NCT06352216 id: Elo-Ger-2023-1642 briefTitle: Prevalence of Synovitis in Patients With Haemophilia A acronym: SynoPrev overallStatus: RECRUITING date: 2024-04-15 date: 2027-02 date: 2027-03 date: 2024-04-08 date: 2024-04-16 name: University Hospital, Bonn class: OTHER name: Swedish Orphan Biovitrum... |
<|newrecord|> nctId: NCT06352203 id: AUT/23.02 briefTitle: Effect of Probiotics on the Intestinal Microbiota of Pediatric Patients overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-09 date: 2025-11 date: 2024-04-08 date: 2024-04-08 name: ProbiSearch SL class: INDUSTRY briefSummary: Numerous studies have descri... |
An interventional, randomised, double-blind, placebo-controlled study will be conducted to investigate the effect of a probiotic supplement on the microbiota composition of children aged 3-7 years with neurodevelopmental issues. |
The duration of the study will be of 6 months approximately, including 6 months of product intake. |
Participants will be randomly assigned to one of the two study groups: control group with placebo administration or probiotic administration group. conditions: Neurodevelopmental Disorders studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: TRIPLE w... |
<|newrecord|> nctId: NCT06352190 id: SY-5007-I-04 briefTitle: A Study to Evaluate the Mass Balance of [14C] SY-5007 in Healthy Adult Male Subjects in China overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2024-06-01 date: 2024-06-01 date: 2024-04-08 date: 2024-04-08 name: Shouyao Holdings (Beijing) Co. LTD clas... |
<|newrecord|> nctId: NCT06352177 id: protocol-1 briefTitle: Digital Therapeutic Lifestyle Intervention Program for Patients With MASLD acronym: ENLIGHTEN overallStatus: NOT_YET_RECRUITING date: 2025-04-01 date: 2029-12-31 date: 2030-08-01 date: 2024-04-08 date: 2024-04-08 name: Milton S. Hershey Medical Center class: O... |
This is a randomized, controlled trial comparing DTx lifestyle intervention in participants with non-cirrhotic MASH to standard clinical care. The study includes a screening period (up to 2 wks.) followed by randomization, 48-wk treatment period and 12-wk follow-up period (total duration up to 62 wks.). conditions: NAS... |
<|newrecord|> nctId: NCT06352164 id: ZYS2024-03 briefTitle: Efficacy Classification Prediction of the Effects of Acupuncture on Abdominal Pain in Patients With Crohn's Disease overallStatus: COMPLETED date: 2015-03-01 date: 2023-12-31 date: 2024-03-31 date: 2024-04-08 date: 2024-04-09 name: Shanghai Institute of Acupun... |
<|newrecord|> nctId: NCT06352151 id: 2022-041 briefTitle: Effects of Orofacial Therapy and Therapeutic Yoga in Children With Down Syndrome overallStatus: RECRUITING date: 2023-10-01 date: 2024-09-28 date: 2024-12-30 date: 2024-04-08 date: 2024-04-09 name: Hasan Kalyoncu University class: OTHER briefSummary: The study a... |
<|newrecord|> nctId: NCT06352138 id: ENCASE briefTitle: Comparative Study of Two Recombinant Human Erythropoietin Products on Chronic Kidney Disease Patients acronym: ENCASE overallStatus: NOT_YET_RECRUITING date: 2024-07 date: 2027-03 date: 2027-03 date: 2024-04-08 date: 2024-04-08 name: Megalabs class: INDUSTRY name:... |
<|newrecord|> nctId: NCT06352125 id: TP-CLN-100503 briefTitle: An Observational Trial to Assess the Performance of the TEG® 6s Diagnostic System With the Citrated K, KH, RTH, FFH Cartridge overallStatus: COMPLETED date: 2021-12-09 date: 2023-01-31 date: 2023-01-31 date: 2024-04-08 date: 2024-04-08 name: Haemonetics Cor... |
<|newrecord|> nctId: NCT06352112 id: 02.04.2024 - POP briefTitle: Effects of the Hypopressive Exercises in Women With Pelvic Organ Prolapse overallStatus: COMPLETED date: 2023-03-15 date: 2024-01-15 date: 2024-02-15 date: 2024-04-08 date: 2024-04-10 name: Hacettepe University class: OTHER name: Istanbul Training and Re... |
<|newrecord|> nctId: NCT06352099 id: 6315 briefTitle: Dietary Supplementation and Cognitive Functions in the Elderly acronym: ESPINS overallStatus: NOT_YET_RECRUITING date: 2024-05 date: 2024-11 date: 2025-04 date: 2024-04-08 date: 2024-04-08 name: Fondazione Policlinico Universitario Agostino Gemelli IRCCS class: OTHE... |
Age-related evolution is a gradual and continuous process involving a series of physical and cognitive changes, which, however, has no real 'onset' age. In fact, rather than chronological age, the concept of 'elderly' is based on the individual's degree of self-sufficiency and independence. From a biological point of v... |
An important factor in counteracting frailty is nutritional intake. Humans ingest approximately 500 g of chemical compounds daily through their diet, most of which are components of plants or vegetables in general. In addition to the well-known macronutrients (proteins, fats, and carbohydrates) and micronutrients (mine... |
Phytochemical compounds are an extremely diverse set of elements that, when taken at significant levels, have a protective effect on human health. These substances exert various biological functions, such as antioxidant activity, modulation of detoxifying enzymes, stimulation of the immune system, reduction of platelet... |
Among the phytochemical compounds, flavonoids represent a category of polyfunctional substances with high bioactivity, comprising more than 5000 compounds. They possess biochemical properties of functional interest in the nutritional and therapeutic fields; for example, rutin, diosmin, and hesperidin are present in som... |
However, few studies have evaluated the effect of hesperidin and proanthocyanidins on motor, cognitive, and functional aspects in the elderly. |
Altemor® is a food supplement based on micronized diosmin, hesperidin, and herbal extracts that has an important integrative supporting action in optimising blood microcirculation. |
The aim of the study is to evaluate the contribution of dietary supplementation with Altemor® on cognitive function, balance, fatigue, and some domains of quality of life in elderly subjects. conditions: Cognitive Impairment conditions: Old Age; Debility studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED inter... |
<|newrecord|> nctId: NCT06352086 id: STUDY00009227 briefTitle: Understanding Visual Processing After Occipital Stroke overallStatus: NOT_YET_RECRUITING date: 2024-09 date: 2028-09 date: 2029-09 date: 2024-04-08 date: 2024-04-08 name: University of Rochester class: OTHER briefSummary: The purpose of this study is to inv... |
<|newrecord|> nctId: NCT06352073 id: 23-2625 id: R668-EE-2380 type: OTHER domain: Regeneron briefTitle: Dupilumab for Eosinophilic Esophagitis With Severe Strictures acronym: DESTRICT overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2025-11 date: 2026-04 date: 2024-04-08 date: 2024-04-08 name: University of North ... |
Participants will have a screening visit where they will complete surveys and undergo an endoscopy (EGD). Blood and biopsies (small tissue samples) will also be collected. If eligible and enrolled into the study, participants will receive weekly subcutaneous (under the skin) injections of dupilumab for 52 weeks (one ye... |
Participants will return for study visits every at weeks 4, 8, 12, 18, 24, 30, 36, 44, and 52. During these visits, vital signs (temperature, heart rate, etc.) will be collected and participants will complete surveys. During visits at week 12, 24, and 52, blood will be collected and an endoscopy with biopsy will be per... |
At 64 weeks (12 weeks after the last dose of dupilumab), participants assigned male at birth (AMAB) will be contacted about their / their partner's pregnancy status and participants assigned female at birth (AFAB) may be asked to come for an in-person visit to complete a urine pregnancy test. conditions: Eosinophilic E... |
<|newrecord|> nctId: NCT06352060 id: KCHRRF_MONITOR AF_030 briefTitle: Dynamic Data-Driven Management of Atrial Fibrillation Using Implantable Cardiac Monitors: The MONITOR-AF Study overallStatus: RECRUITING date: 2024-04 date: 2024-06 date: 2024-09 date: 2024-04-08 date: 2024-04-08 name: Kansas City Heart Rhythm Resea... |
<|newrecord|> nctId: NCT06352047 id: Karadeniz Tech. University briefTitle: The Effects of Positioning After Extubation of Preterm Infants on the Respiratory Functions overallStatus: COMPLETED date: 2018-11-01 date: 2019-06-01 date: 2019-06-01 date: 2024-04-08 date: 2024-04-08 name: Karadeniz Technical University class... |
Hypothesis 0a (H0a): There is no difference between the oxygen saturation (SpO2) levels of preterm infants in supine and prone positions after extubation. |
Hypothesis 0b (H0b): There is no difference between the respiratory rate of preterm infants in supine and prone positions after extubation. |
Hypothesis 0c (H0c): There is no difference between the respiratory rhythms of preterm infants in supine and prone positions after extubation. |
Hypothesis 0d (H0d): There is no difference between respiratory distress in preterm infants in supine and prone positions after extubation. conditions: Premature Infants studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL interventionModelDescription: Simple randomization method was ... |
<|newrecord|> nctId: NCT06352034 id: Empathy Training for Students briefTitle: Empathy Training for Future Mental Health Practitioners in University Students overallStatus: NOT_YET_RECRUITING date: 2024-03-30 date: 2024-04-30 date: 2024-10-01 date: 2024-04-08 date: 2024-04-08 name: Peking University class: OTHER briefS... |
<|newrecord|> nctId: NCT06352021 id: KAHRİMAN İlknur briefTitle: The Effect of Distraction With a Kaleidoscope on the Level of Perceived Pain During Blood Sampling in Children overallStatus: COMPLETED date: 2019-05-30 date: 2019-06-30 date: 2019-06-30 date: 2024-04-08 date: 2024-04-08 name: İlknur KAHRİMAN class: OTHER... |
Hypothesis 0 (H0): There is no difference between the pain scores of the kaleidoscope group and the control group during blood sampling. |
Hypothesis 1 (H1): There is a difference between the pain scores of the kaleidoscope group and the control group during blood sampling. conditions: Pain studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: PREVENTION masking: SINGLE whoMasked: OUTCOMES_ASSESSOR count: ... |
<|newrecord|> nctId: NCT06352008 id: Zhansheng Jiang briefTitle: To Evaluate the Efficacy and Safety of Anrotinib Hydrochloride Capsule in Postoperative Non-pCR Patients With Non-small Cell Lung Cancer overallStatus: NOT_YET_RECRUITING date: 2024-06-01 date: 2025-06-01 date: 2026-06-01 date: 2024-04-08 date: 2024-04-08... |
<|newrecord|> nctId: NCT06351995 id: KOR-19-22 briefTitle: Neostigmine and Glycopyrrolate by Iontophoresis overallStatus: ACTIVE_NOT_RECRUITING date: 2020-11-06 date: 2022-10-25 date: 2025-01-01 date: 2024-04-08 date: 2024-04-08 name: James J. Peters Veterans Affairs Medical Center class: FED briefSummary: To determine... |
<|newrecord|> nctId: NCT06351982 id: 211123PER3-3-2 briefTitle: Treatment Of Shallow Periodontal Pockets 4-6mm Using AIRFLOW Prophylaxis Master Device With Erythritol vs Manual Scalers overallStatus: RECRUITING date: 2024-03-01 date: 2025-06-01 date: 2026-01-01 date: 2024-04-08 date: 2024-04-08 name: Cairo University c... |
Both hand and ultrasonic instruments are characterized by being time-consuming and requiring technical skill, often causing patient discomfort and post-treatment pain, including hypersensitivity resulting from the loss of hard tissue when scaling the tooth surface. Ultrasonic instruments tend to leave a rougher surface... |
The aim of this study is to evaluate changes in probing depth clinically, Bleeding on probing, Clinical attachment level, Plaque index, Calculus index, Patient pain/discomfort, Patient satisfaction, Cost effectiveness, Treatment time and Number of pockets closed after using AIRFLOW® Prophylaxis Master device with eryth... |
<|newrecord|> nctId: NCT06351969 id: Ms 9-12-2023 briefTitle: Evaluating Placental Thickness and Thickness of Uterine Muscle at Placenta Attachment in Prediction of Postpartum Blood Loss overallStatus: RECRUITING date: 2023-12-21 date: 2024-12 date: 2024-12 date: 2024-04-08 date: 2024-04-08 name: Benha University class... |
<|newrecord|> nctId: NCT06351956 id: Arrhythmias in Septic Patients briefTitle: New Onset Cardiac Arrhythmias in Septic Patients in Critical Care Setting, Predictors and Outcomes. overallStatus: NOT_YET_RECRUITING date: 2024-04-20 date: 2026-04-20 date: 2026-12-30 date: 2024-04-08 date: 2024-04-08 name: Assiut Universi... |
<|newrecord|> nctId: NCT06351943 id: ImageDB pilot briefTitle: Proximal Femur Image Database Validation overallStatus: ACTIVE_NOT_RECRUITING date: 2021-05-01 date: 2024-10-01 date: 2025-06-30 date: 2024-04-08 date: 2024-04-08 name: AO Innovation Translation Center class: OTHER name: University of Turin, Italy briefSumm... |
The goal of this project is to determine the agreement between the Turin annotation of fracture status and the annotation from an external group of AO expert surgeons for a random subset of the Turin images. conditions: Proximal Femoral Fracture studyType: OBSERVATIONAL observationalModel: OTHER timePerspective: CROSS_... |
<|newrecord|> nctId: NCT06351930 id: EA210473 briefTitle: CBT for Insomnia in Adolescents With ADHD overallStatus: RECRUITING date: 2023-01-01 date: 2025-12-31 date: 2025-12-31 date: 2024-04-08 date: 2024-04-08 name: The University of Hong Kong class: OTHER name: Kwai Chung Hospital, Hong Kong briefSummary: Insomnia an... |
<|newrecord|> nctId: NCT06351917 id: LEVEXE briefTitle: Effect of Topical PlexoZome® Levagen® Spray on Relief of Post Exercise Knee Joint Pain overallStatus: NOT_YET_RECRUITING date: 2024-05-01 date: 2025-04-01 date: 2025-05-01 date: 2024-04-08 date: 2024-04-10 name: RDC Clinical Pty Ltd class: INDUSTRY briefSummary: T... |
<|newrecord|> nctId: NCT06351904 id: RAG-01-01 briefTitle: A Study of RAG-01 in Patients With Non-muscle-invasive Bladder Cancer (NMIBC) Who Have Failed Bacillus Calmette Guérin (BCG) Therapy overallStatus: RECRUITING date: 2024-04-03 date: 2025-06-30 date: 2025-08-31 date: 2024-04-08 date: 2024-04-16 name: Ractigen Th... |
<|newrecord|> nctId: NCT06351891 id: SHARE2402 briefTitle: Efficacy and Safety of Bismuth Quadruple Therapy Containing Cefuroxime and Tetracycline as First-line Therapy for Eradicating Helicobacter Pylori in Patients Allergic to Penicillin overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2024-12 date: 2024-12 date... |
<|newrecord|> nctId: NCT06351878 id: Pro00113559 briefTitle: TipTraQ Home Sleep Test Validation Study overallStatus: RECRUITING date: 2024-02-28 date: 2024-08-23 date: 2024-08-23 date: 2024-04-08 date: 2024-04-08 name: PranaQ Pte. Ltd. class: INDUSTRY briefSummary: A validation study has been designed to assess the per... |
<|newrecord|> nctId: NCT06351865 id: PHU/2023/21 briefTitle: Feasibility Study to Evaluate the Use of Patient Reported Complications After Digital Consent acronym: PRC overallStatus: RECRUITING date: 2024-03-07 date: 2024-09-19 date: 2024-10-31 date: 2024-04-08 date: 2024-04-09 name: Portsmouth Hospitals NHS Trust clas... |
<|newrecord|> nctId: NCT06351852 id: 1678243 briefTitle: Transdermal Administration by a Novel Wireless Iontophoresis Device overallStatus: RECRUITING date: 2022-03-22 date: 2025-02-15 date: 2025-02-15 date: 2024-04-08 date: 2024-04-08 name: James J. Peters Veterans Affairs Medical Center class: FED briefSummary: Perso... |
The ability to move the bowel contents along to the rectum was severely impaired primary because of poor gut contractions on the left side of the colon, as shown by our team of investigators. To address this problem, a dual medication combination (neostigmine and glycopyrrolate) was developed that safely and predictabl... |
The proposed research project to determine the safety of positively charged compounds (e.g., vitamin B12, NEO, and GLY) administered transcutaneously by the prototype wireless ION device and to compare the pharmacokinetic profiles of transcutaneous administration of NEO and GLY by the wireless ION device to a commercia... |
<|newrecord|> nctId: NCT06351839 id: 2024/500457(REK) briefTitle: Sleep Well Despite Persistent Pain Symptoms acronym: Sleep-Well overallStatus: NOT_YET_RECRUITING date: 2024-10 date: 2026-12 date: 2027-12 date: 2024-04-08 date: 2024-04-08 name: University of Tromso class: OTHER name: University Hospital of North Norwa... |
Eligible patients: Investigators target adult patients referred to the University Hospital of North Norway (Tromsø) for a diagnostic evaluation of their pain condition. Patients eligible for the Sleep-Well study are those who satisfy diagnostic criteria for a non-malign pain disorder plus a comorbid insomnia sleep diso... |
Aims: This trial uses a randomized semi-crossover design to examine if the Sleep-Well group does better regarding insomnia and sleep quality than the control patients (TAU). The primary outcome measures are reductions in diagnostic criteria for insomnia, self-reported insomnia symptoms, quality of life, and actigraphy-... |
The intervention: The Sleep-Well program schedules group sessions that cover four topics (sleep literacy, behavioural and mental strategies, maintenance and relapse prevention). All sessions are led by two therapists. Those randomized to the active control group (TAU) cross over to the Sleep-Well intervention three mon... |
<|newrecord|> nctId: NCT06351826 id: 22070876 briefTitle: Effectiveness of ELLASI Intervention Towards Polytrauma Patients in the Emergency Department overallStatus: RECRUITING date: 2024-01-03 date: 2024-04 date: 2024-05 date: 2024-04-08 date: 2024-04-08 name: Indonesia University class: OTHER briefSummary: This clini... |
1. Is the response time of polytrauma patients who receive ELLASI in the intervention group faster than the control group? |
2. Is the deterioration score of polytrauma patients who receive ELLASI in the intervention group better than the control group? |
3. Is the metabolic status of polytrauma patients who receive ELLASI in the intervention group better than the control group? |
Polytrauma patients in the intervention group will receive ELLASI, a structured intervention consisting of the six following: |
1. Evaluation of airway and cervical control, remove the foreign body, fluid, etc., from the airway, |
2. Patient positioning and giving oxygen, head-up, |
3. Stabilisation, including IV insertion, applying pressure and bandage, place monitor, and haemodynamic monitoring |
4. Assessment: re-assessment of pain and other main complaints |
5. Make sure informed consents are documented |
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