Clinical trials: Demonstrate Effectiveness of Virtual Simulator in Improving or Performance
Chronic Non-specific Low Back Pain
Isokinetic Profile of Ankle Joint Muscles in Chronic Non Specific Low Back Pain Patients
Chronic non-specific low back pain and its resulting infirmity have become a huge health and socioeconomic burden. Low back pain is reportedly associated with decreased activities of daily living and quality of life.
- Trial name
- NCT07636967
- Testing
- Humac Isokinetic 2015 System 2
- Where
- Egypt
- Volunteers
- 50 people
- Sponsor
- Cairo University
Physical Activity
The Impact of Exercise With Blood Flow Restriction: Sex and Age Differences
The primary objective is to investigate whether six weeks of resistance training, in combination with blood flow restriction, produces a different adaptation in fat-free mass between males and females that are not physically…
- Trial name
- NCT05615831
- Testing
- Resistance Training with Blood flow restriction
- Where
- Canada
- Volunteers
- 72 people, healthy volunteers welcome
- Sponsor
- University of New Brunswick
Athletic Performance, Neuromuscular Training
Comparison of Combined Sprint-Plyometric Training Versus Traditional Strength Training on Speed, Agility, Power, and Movement Quality in Intermediate Rugby Players
Comparison of Combined Sprint-Plyometric Training Versus Traditional Strength Training on Speed, Agility, Power, and Movement Quality in Intermediate Rugby Players: A Randomized Controlled Trial
- Trial name
- NCT07591675
- Testing
- Combined Sprint-Plyometric Training, Traditional Strength Training Group
- Where
- Pakistan
- Volunteers
- 64 people, healthy volunteers welcome
- Sponsor
- Ibadat International University, Islamabad
Metabolism, Exercise
Capsaicinoid Ingestion, Human Metabolism and Exercise (Phase 2)
Capsaicinoids (the active ingredient in hot peppers) have been shown to cause a moderate increase in energy expenditure (50 kcal/day) as well as reductions in appetite, energy intake, and (visceral) adiposity.
- Trial name
- NCT02138630
- Testing
- Capsaicin
- Where
- Canada
- Volunteers
- healthy volunteers welcome
- Sponsor
- University of Prince Edward Island
Healthy Subjects, Male or Female, of 18-60 Years Old, With Phototype I, II or III, Not Pre-treated/Pre-protected Skin
Performance of Different Application Regimens of ACTINICA® on Protection From UVR-induced Erythema After One Day of Sun Exposure in Fair-skinned Healthy Subjects.
Study objective To assess the performance of different application regimens of Actinica® on protection from UV rays-induced erythema throughout 1 day of sun exposure in fair-skinned healthy subjects (phototype I to III).
- Trial name
- NCT02251756
- Testing
- Actinica, 0.8 mg/cm2, 1 application, Actinica, 0.8 mg/cm2, 2 applications, Actinica, 2 mg/cm2, 1 application
- Where
- France
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Galderma R&D
Sports Physical Therapy
Integration of the Wingate Test Into Virtual Reality Based System
Virtual reality (VR) is a technology utilizing three-dimensional graphical representations to immerse individuals in computer-generated environments, fostering engagement through visual, auditory, and tactile stimuli.
- Trial name
- NCT06661395
- Testing
- Wingate Anaerobic Test with Virtual Reality
- Where
- Turkey (Türkiye)
- Volunteers
- 30 people, healthy volunteers welcome
- Sponsor
- Istanbul Medipol University Hospital
Complex Abdominal Aortic Aneurysms
Clinical Performance and Safety Assessment of the Use of iCover Balloon Expandable Covered Stent (iVascular) Implanted as Bridging Stent in FEVAR (Fenestrated Endovascular Aortic Repair) for the Treatment of Complex Abdominal Aortic Aneurysms
fenCo is a European multicentre, prospective study to evaluate the use of the iCover covered stents as bridging stents for reno-visceral target vessel during fEVAR for the treatment of complex abdominal aortic aneurysms.
- Trial name
- fenCo (NCT07529275)
- Testing
- iCover balloon-expandable covered peripheral stent system as bridging stent
- Where
- 24 sites in Belgium, France and 3 more
- Volunteers
- 165 people
- Sponsor
- iVascular S.L.U.
Sepsis
Evaluating the Diagnostic Performance and Impact on Clinical Outcomes of the NuRapid-CRISPR Pathogen Profile Assay in ICU Patients With Sepsis
This study is a prospective, multicenter, integrated trial designed to evaluate, from the perspectives of diagnostic performance and clinical utility, whether a diagnostic and treatment strategy based on the NuRapid-CRISPR rapid…
- Trial name
- NCT07580001
- Testing
- NuRapid-CRISPR Rapid Pathogen Detection Technology, Traditional pathogen culture
- Where
- 3 sites in China
- Volunteers
- 396 people
- Sponsor
- Shanghai 10th People's Hospital
Pancreatic Cancer
CPI-613 in Combination With Modified FOLFIRINOX in Locally Advanced Pancreatic Cancer
The purpose of this study is to treat participants with the combination of CPI-613 (the study drug) with FOLFIRINOX (the standard combination of drugs) to determine if it is safe and effective for participants with localized and…
- Trial name
- NCT03699319
- Testing
- CPI 613, Oxaliplatin, Irinotecan
- Where
- United States
- Volunteers
- 49 people
- Sponsor
- David Bajor, MD
Diabetes
Evaluation of an Investigational Blood Glucose Monitoring System
The purpose of this study was to determine if untrained subjects who have diabetes can operate the Investigational Blood Glucose Monitoring System (BGMS) and obtain valid glucose results.
- Trial name
- NCT01859494
- Testing
- NINJA 3 Investigational Blood Glucose Monitoring System
- Where
- 2 sites in United States
- Volunteers
- 219 people
- Sponsor
- Ascensia Diabetes Care
Nocturia
Daytime Impact Sleep Study
This trial will investigate the relationship of sleep, daytime performance and nocturia in patients treated with Desmopressin or placebo.
- Trial name
- DAISS (NCT01779466)
- Testing
- Desmopressin
- Where
- United Kingdom
- Volunteers
- 5 people
- Sponsor
- Ferring Pharmaceuticals
Lung Transplantation, End Stage Lung Disease
Respiratory, Limb Muscle Properties, and Physical Performance in Adult Lung Transplant Recipients
The goal of this observational study is to evaluate respiratory and limb muscle properties in adults awaiting lung transplantation and determine how these measures relate to physical performance, symptoms, and recovery after…
- Trial name
- NCT07747337
- Testing
- Respiratory and Limb Muscle Assessment
- Where
- United States
- Volunteers
- 36 people
- Sponsor
- University of Florida
Cognitive Performance During Physical Activity
Cognition in Motion
The purpose of this study is to evaluate the effect of low-intensity exercise on cognitive functioning during activity. Evaluation was accomplished by having participants perform standardized cognitive tests while in three forms…
- Trial name
- CIM (NCT02927275)
- Testing
- Experimental: Standing Modality, Experimental: Biking Modality, Experimental: Walking Modality
- Where
- United States
- Volunteers
- 88 people, healthy volunteers welcome
- Sponsor
- Baylor College of Medicine
Prostate Cancer
Diagnostic Performance Of Non-Endorectal Coil Multiparametric Magnetic Resonance Imaging Of Prostate With Flexible AIR Coil (DoNEMAC Study)
Multiparametric MRI (mpMRI) of the prostate is an important tool for diagnosis of clinically significant prostate cancer (csPCa) in men with an elevated serum prostate specific antigen, which can decrease the rate of unnecessary…
- Trial name
- NCT05043012
- Testing
- flexible AIR coil, endorectal coi
- Where
- United States
- Volunteers
- 258 people
- Sponsor
- M.D. Anderson Cancer Center
Anemia, Iron Deficiency
Efficacy of Double Fortified Salt (DFS) to Improve Work Productivity in Women in India
The main objective of the present study is to assess the impact of double fortified salt containing iron and iodine on work performance (productivity) of women plantation workers in India.
- Trial name
- DFS (NCT01032005)
- Testing
- double fortified salt
- Where
- India
- Volunteers
- 248 people, healthy volunteers welcome
- Sponsor
- Micronutrient Initiative
Resectable Colorectal Carcinoma, Stage II Colorectal Cancer AJCC v8
Minimal Residual Disease Testing for the Early Detection of Cancer Recurrence in Resectable Stage II-IV Colorectal Cancer Patients
This clinical trial compares minimal residual disease (MRD) testing with the Haystack blood test (assay) to the Signatera® assay for the early detection of the cancer returning (cancer recurrence) in patients with stage II-IV…
- Conditions
- Resectable Colorectal Carcinoma, Stage II Colorectal Cancer AJCC v8, Stage III Colorectal Cancer AJCC v8, Stage IV Colorectal Cancer AJCC v8
- Trial name
- NCT07125729
- Testing
- Biospecimen Collection, cfDNA or ctDNA Measurement, Electronic Health Record Review
- Where
- 13 sites in United States
- Volunteers
- 150 people
- Sponsor
- City of Hope Medical Center
Heart Failure
Pilot Feasibility Study of the Safety and Efficacy of Anakinra in Heart Failure With Preserved Ejection Fraction
This will be a randomized, double-blind, crossover pilot study to measure the safety and feasibility of Interleukin-1 (IL-1) blockade with Anakinra in patients with stable heart failure with preserved ejection fraction.
- Trial name
- NCT01542502
- Testing
- Anakinra
- Where
- United States
- Volunteers
- 12 people
- Sponsor
- Virginia Commonwealth University
Stroke
Effects of Otago Exercise Program in Falls, Balance and Physical Performance in Stroke Patients
This study aims to determine the effects of the Otago Exercise Program (OEP) on falls and balance as well as overall physical performance. Participants will be divided into two groups; control and intervention group.
- Trial name
- NCT06426862
- Testing
- Otago Exercise Program, Control Group
- Where
- Pakistan
- Volunteers
- 30 people
- Sponsor
- Riphah International University
Healthy
Clinical Performance of Masimo INVSENSOR00057 for Heart Rate Measurements
This study is designed to compare the accuracy of a noninvasive measurement of heart rate compared to reference values obtained by a standard of care ECG monitor.
- Trial name
- NCT05462886
- Testing
- Masimo INVSENSOR00057
- Where
- United States
- Volunteers
- 86 people, healthy volunteers welcome
- Sponsor
- Masimo Corporation
Sleep
Evaluation of SmartSleep Technology for Improving the Efficiency and Restorative Quality of Sleep in Healthy Adults
This study aims to assess whether slow wave sleep enhancement using SmartSleep technology benefits daytime cognitive performance during periods of chronic sleep restriction.
- Trial name
- NCT03911154
- Testing
- Philips SmartSleep Technology--Continuous Fixed Interval modality, Philips SmartSleep Technology--Block modality, Philips SmartSleep Technology--In-Phase Adjustable modality
- Where
- United States
- Volunteers
- 9 people, healthy volunteers welcome
- Sponsor
- University of Pennsylvania
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