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<|newrecord|> nctId: NCT06332950 id: MA-SCLC-II-015 briefTitle: Safety and Efficacy of Adebrelimab Plus Irinotecan Liposome (II) With or Without Famitinib in ES-SCLC Pre-treated With Immunotherapy overallStatus: NOT_YET_RECRUITING date: 2024-04-01 date: 2027-04-01 date: 2027-04-01 date: 2024-03-27 date: 2024-03-27 name... |
<|newrecord|> nctId: NCT06332937 id: H-2102-079-1197 briefTitle: Breast Reconstruction overallStatus: ACTIVE_NOT_RECRUITING date: 2021-02-22 date: 2023-12-15 date: 2024-12-31 date: 2024-03-27 date: 2024-03-27 name: Seoul National University Hospital class: OTHER briefSummary: Complications following postmastectomy brea... |
<|newrecord|> nctId: NCT06332924 id: 2023/19 briefTitle: Primipara Pregnant Women and Motivational Interview overallStatus: NOT_YET_RECRUITING date: 2024-04-01 date: 2024-07-01 date: 2024-08-01 date: 2024-03-27 date: 2024-03-27 name: Saglik Bilimleri Universitesi class: OTHER briefSummary: The first birth is the most i... |
This planned study was planned as a randomized controlled trial with pre-test and post-test measurements, with the aim of determining the level of traumatic birth perception in primipara women who were given or not given training and examining the effects of positive birth motivational education by taking into account ... |
<|newrecord|> nctId: NCT06332911 id: RO-231129 briefTitle: Shockwave™Peripheral Intravascular Lithotripsy Balloon for Advanced Endovascular Aortic Repair acronym: TEVAR overallStatus: NOT_YET_RECRUITING date: 2024-08-01 date: 2025-08-30 date: 2026-08-30 date: 2024-03-27 date: 2024-03-27 name: Rede Optimus Hospitalar SA... |
The aim of this study is to evaluate the outcomes of the Shockwave™ Peripheral Intravascular Lithotripsy Balloon (Shockwave Medical Inc.) in the routine treatment of hostile iliac accesses during TEVAR and F/BEVAR. conditions: Thoracoabdominal Aortic Aneurysm, Without Mention of Rupture conditions: Abdominal Aortic Ane... |
<|newrecord|> nctId: NCT06332898 id: AG-01-0324 briefTitle: The Effects of a Nutritional Supplement on Nutrient Status and Quality of Life overallStatus: NOT_YET_RECRUITING date: 2024-03-31 date: 2024-10-31 date: 2025-02-04 date: 2024-03-27 date: 2024-04-01 name: Athletic Greens International class: INDUSTRY name: Citr... |
<|newrecord|> nctId: NCT06332885 id: 630-2001-01 briefTitle: Zephyr Valve Japan Post-Marketing Surveillance overallStatus: RECRUITING date: 2024-03-12 date: 2027-03-31 date: 2028-03-31 date: 2024-03-27 date: 2024-04-19 name: Pulmonx Corporation class: INDUSTRY briefSummary: This is a multicenter, prospective, observati... |
<|newrecord|> nctId: NCT06332872 id: M046q/66 briefTitle: Comparison Effectiveness of Oral Ivermectin , 1% Permethrin Shampoo and 4% Dimeticone Liquid Gel in the Treatment of Pediculosis Capitis Among School Children in Chachoengsao Province, Thailand overallStatus: ACTIVE_NOT_RECRUITING date: 2023-12-15 date: 2024-03-... |
The main questions it aims to answer are |
* What is more effective between Oral ivermectin , 1% Permethrin shampoo and 4%Dimeticone liquid gel in the treatment of Pediculosis capitis in school children in Baan Nayao, Chachoengsao Province, Thailand? |
* What is Prevalence and risk factors of being infected with in head lice in school and community? |
* What is Side effects of Oral ivermectin , 1% Permethrin shampoo and 4%Dimeticone liquid gel? |
Participants will receive three different drugs are |
* oral ivermectin |
* 4% Dimeticone liquid gel |
* 1% Permethrin shampoo |
Participants voluntarily received oral ivermectin as per medical prescription, with treatment outcomes, side effects, and satisfaction levels monitored following two treatment cycles. Those exhibiting persistent lice infestations were subsequently treated with 1% permethrin shampoo, the standard treatment, while altern... |
<|newrecord|> nctId: NCT06332859 id: FOR-0022 briefTitle: Effectiveness of a Resilience-Based Rehabilitation Program for Patients With Coronary Heart Disease overallStatus: NOT_YET_RECRUITING date: 2024-04-15 date: 2026-10-14 date: 2026-10-14 date: 2024-03-27 date: 2024-03-27 name: Pensionsversicherungsanstalt class: O... |
<|newrecord|> nctId: NCT06332846 id: KB-0012/06/10 briefTitle: Oral Health in Patients Hospitalized Because of Ischemic Stroke overallStatus: COMPLETED date: 2019-10-10 date: 2021-11-15 date: 2023-12-10 date: 2024-03-27 date: 2024-03-27 name: Pomeranian Medical University Szczecin class: OTHER briefSummary: Maintaining... |
The oral health was assessed in patients with stroke and in (control group). The following elements were assessed: missing teeth, the presence of active caries foci, the presence of existing fillings and prosthetic restorations. To assess oral hygiene API (Approximal Plaque Index) was used. As part of periodontal exami... |
<|newrecord|> nctId: NCT06332833 id: 235 briefTitle: Availability of Venous Conduits in Patients With Varicose Veins for Arterial Bypass Surgery overallStatus: RECRUITING date: 2023-12-01 date: 2024-05-31 date: 2024-05-31 date: 2024-03-27 date: 2024-03-27 name: Pirogov Russian National Research Medical University class... |
<|newrecord|> nctId: NCT06332820 id: 202401226RINB briefTitle: In Patients With Obstructive Airway Disease, Investigate the Effects of Different Breathing Strategies and Pedaling Rates on the Physiological Response to Bicycle Exercise overallStatus: ACTIVE_NOT_RECRUITING date: 2024-03-20 date: 2030-12-31 date: 2030-12-... |
<|newrecord|> nctId: NCT06332807 id: NGGT002-P-2301 briefTitle: AAV Gene Therapy Clinical Study in Adult Classic PKU overallStatus: NOT_YET_RECRUITING date: 2024-05-22 date: 2030-12-30 date: 2030-12-30 date: 2024-03-27 date: 2024-03-27 name: NGGT (Suzhou) Biotechnology Co., Ltd. class: INDUSTRY briefSummary: This is a ... |
Participants will receive a single administration of NGGT002 and will be followed for safety and efficacy for 5 years. conditions: Phenylketonurias studyType: INTERVENTIONAL phases: PHASE1 phases: PHASE2 allocation: NA interventionModel: SINGLE_GROUP primaryPurpose: TREATMENT masking: NONE count: 12 type: ESTIMATED nam... |
<|newrecord|> nctId: NCT06332794 id: H-2201 briefTitle: Keep On Keep Up for Parkinson's acronym: KOKU4PD overallStatus: NOT_YET_RECRUITING date: 2024-06-03 date: 2025-03-01 date: 2025-06-30 date: 2024-03-27 date: 2024-04-24 name: Northumbria University class: OTHER name: University of Manchester name: Northumbria Healt... |
The main aims of the study are to: |
1. To explore the usability and acceptability of the PD specific KOKU programme from a user and health care professional perspective. |
2. To produce a KOKU4PD digital program that is ready for National Health Service (NHS) approval and a future effectiveness evaluation. |
Participants will use the KOKU4PD app at home for 4 weeks. They will be assessed at baseline and after the 4 weeks to measure aspects of their disease status, mobility, thinking, mood and quality of life. They will also be asked to complete some questionnaires about the usability of the app. conditions: Parkinson's Dis... |
<|newrecord|> nctId: NCT06332781 id: 2126175 briefTitle: Intravesical Gentamicin to Prevent Recurrent UTI overallStatus: NOT_YET_RECRUITING date: 2024-08-01 date: 2025-06-01 date: 2025-07-31 date: 2024-03-27 date: 2024-03-28 name: Women and Infants Hospital of Rhode Island class: OTHER briefSummary: Feasibility assessm... |
<|newrecord|> nctId: NCT06332768 id: WEAN_2021 briefTitle: NIV Versus HFO Versus Standard Therapy Immediately After Weaning From Mechanical Ventilation in ARDS Patients overallStatus: COMPLETED date: 2017-09-01 date: 2022-01-01 date: 2022-03-01 date: 2024-03-27 date: 2024-03-27 name: Northern State Medical University c... |
<|newrecord|> nctId: NCT06332755 id: LG-LRCL001 briefTitle: Study to Evaluate LB-LR1109 for the Treatment of Solid Tumors acronym: LB-LR1109 overallStatus: NOT_YET_RECRUITING date: 2024-05 date: 2025-11 date: 2027-02 date: 2024-03-27 date: 2024-03-27 name: LG Chem class: INDUSTRY briefSummary: This is a Phase 1, first-... |
<|newrecord|> nctId: NCT06332742 id: QXZS for DOR briefTitle: Real-world Evaluation of Qingxin Zishen Decoction on Ovarian Reserve Function Clinical Efficacy in Patients With Decreased overallStatus: RECRUITING date: 2023-11-01 date: 2026-12-31 date: 2026-12-31 date: 2024-03-27 date: 2024-04-04 name: Yun Chen class: OT... |
<|newrecord|> nctId: NCT06332729 id: EG,KFS,lab reserach 6 briefTitle: Universal Exercise Unit Versus Functional Electrical Stimulation On Genu Recurvatum In Diplegic Cerebral Palsy overallStatus: RECRUITING date: 2024-02-01 date: 2024-05-15 date: 2024-06-15 date: 2024-03-27 date: 2024-03-27 name: Mahmoud Reda Elsharka... |
Inclusion Criteria: |
* Children aged four to eight years. |
* Grade of spasticity ranging from 1 to 1+ on the Modified Ashworth scale. |
* Classified as Level I or II on the Gross Motor Functional Classification System (GMFCS). |
* Ability to follow verbal commands and instructions. |
Exclusion Criteria: |
* Previous neurological or orthopedic surgery in the lower extremities. |
* Botox injection in the lower extremities within the past six months. |
* Fixed deformity in the joints of the lower limb. |
* Genu recarvatum secondary to surgery. |
* Severe hearing and visual defects. |
Materials for Subject Selection and Evaluation: |
* Modified Ashworth Scale for muscle tone assessment. |
* Gross Motor Functional Classification System (GMFCS) for functional activity classification. |
* Digital goniometer for measuring the angle of knee hyperextension. |
* Lafayette Manual Muscle Tester for quantifying muscle strength. |
Methods: |
* Assessment of muscle tone using the Modified Ashworth Scale, evaluating spasticity in calf muscles and hip/knee extensors. |
* Evaluation of gross motor function using the GMFCS. |
* Assessment of genu recarvatum using a digital goniometer. |
* Assessment of muscle strength using the Lafayette Manual Muscle Tester, focusing on hamstrings and tibialis anterior muscles. |
* Assessment of range of motion in the knee joint using Kinovea software. |
* Treatment procedures involving physical therapy sessions with a combination of exercises and interventions tailored to each group (Group A and Group B). |
Group A Treatment: |
- Designed physical therapy program combined with pulley therapy for muscle strengthening. |
Group B Treatment: |
- Designed physical therapy program combined with functional electrical stimulation during walking on a treadmill for muscle stimulation. |
The interventions in both groups aim to improve muscle strength, range of motion, and functional abilities in children with cerebral palsy. conditions: Cerebral Palsy studyType: INTERVENTIONAL phases: NA allocation: RANDOMIZED interventionModel: PARALLEL primaryPurpose: TREATMENT masking: SINGLE whoMasked: PARTICIPANT ... |
<|newrecord|> nctId: NCT06332716 id: KY20222234 briefTitle: Research on the Correlation Between Organoid Drug Sensitivity Testing and Precise Treatment of Gastrointestinal Tumors overallStatus: RECRUITING date: 2022-08-26 date: 2025-12 date: 2025-12 date: 2024-03-27 date: 2024-03-27 name: Jianjun Yang,MD class: OTHER b... |
<|newrecord|> nctId: NCT06332703 id: IACA briefTitle: Acanthamoeba and Artificial Intelligence overallStatus: NOT_YET_RECRUITING date: 2024-04 date: 2024-10 date: 2025-04 date: 2024-03-27 date: 2024-03-27 name: IRCCS Ospedale San Raffaele class: OTHER briefSummary: Acanthamoeba keratitis, caused by the pathogen Acantha... |
This observational retrospective and single-center study, of exploratory nature, aims to determine the possibility of identifying patterns that may be useful for future rapid diagnosis of Acanthamoeba keratitis from confocal images, leveraging the normality of corneal examination and the high specificity and sensitivit... |
The data will be based on patients who have been confirmed positive through laboratory tests with proven effectiveness in detecting the infection. |
The laboratory tests considered for the division of patients into their respective groups are bacterial examination, PCR examination, and culture examination. |
Patients were divided into two groups, the first comprising patients positive for Acanthamoeba infection, while the second comprised patients negative for Acanthamoeba but positive for other pathogens. The study will last for 18 months. |
The cohort under study includes 151 patients from the IRCCS San Raffaele Hospital who underwent the aforementioned examinations, of which 76 cases will be included in the group of patients positive for Acanthamoeba and 75 in the group of controls positive for other pathogens. |
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