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NCT ID: NCT05325996 Recruiting - Clinical trials for Glaucoma, Open-Angle

Evaluating Home Testing Devices for the Management of Glaucoma

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

With the advancement in technology we have the opportunity of performing the glaucoma testing at home to monitor the disease. The purpose of this study is evaluating the feasibility and patient acceptance of home testing with head mounted perimetry; detection of progression with head mounted perimetry vs office based perimetry; and monitoring the eye pressure measured by patients at home using a portable tonometer.

NCT ID: NCT05331274 Recruiting - Clinical trials for Chronic Low Back Pain

The Effect of Structured Pain Education on Pain and Performance Parameters in Patients With Chronic Low Back Pain

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

The Effect of Structured Pain Education on Pain and Performance Parameters in Patients with Chronic Low Back Pain The aim of this study is to compare the effects of only Low Load Motor Control Exercises and Pain Education in addition to these exercises on pain, performance, disability and psychological factors, and to present a generalizable pain education in patients with chronic low back pain. We think that DYMK exercises applied together with a general Pain Education given to the patients will provide more improvement on these factors. The patients will be divided into 2 groups, as a pain training group and an exercise group, with 20 people in each group, in a randomized controlled manner. Only DYMK exercise training will be applied to the exercise group. In the pain training group, pain training will be applied in addition to the DYMK exercise training. As an evaluation parameter to the participants; Numerical Rating Scale, Short-Form McGill Pain Questionnaire, Pain Catastrophizing Scale, Tampa Kinesiophobia Scale, Roland-Morris Disability Questionnaire, Pain Self-Efficacy Questionnaire, Passive Lumbar Extension Test, Finger-Place Test and Physical Performance Test Battery will be applied. Patients will be evaluated before the start of the study (T0) and at the end of the study (T1). Low Load Motor Control Exercises will be applied to people in both groups for 4 weeks, 3 days a week, during 20-30 minute sessions. In addition to the DYMK exercise training, a session of 30 to 50 minutes of Pain Training in groups of 4 to 5 people will be given to the patients included in the Pain Training group at the beginning of the exercise training and the exercise training will begin.

NCT ID: NCT05332691 Recruiting - Clinical trials for Hypertrophic Obstructive Cardiomyopathy

Transapical Beating-heart Septal Myectomy in Patient With Hypertrophic Obstructive Cardiomyopathy

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

The primary purpose of this study is to evaluate the feasibility, the safety and the efficacy of the transapical beating-heart septal myectomy for the treatment of hypertrophic obstructive cardiomyopathy. This is a prospective, single-arm, single-center, first-in-man study.

NCT ID: NCT05333367 Recruiting - Clinical trials for Graft Vs Host Disease

MORPHEE : Mechanisms of Cell Death Induced by Extracorporeal Photochemotherapy

MORPHEE
Start date: April 15, 2022
Phase: N/A
Study type: Interventional

The objective of this study is to describe the type of cell death induced by extracorporeal photochemotherapy, depending on the cell type, using a panel of complementary analysis techniques.

NCT ID: NCT05333445 Recruiting - Atrial Fibrillation Clinical Trials

NURSE-led Follow-up in Patients Undergoing CATheter Ablation for Atrial Fibrillation

NURSECAT-AF
Start date: April 15, 2022
Phase: N/A
Study type: Interventional

The study aims to examine the effect of nurse-led education program on quality of life, atrial fibrillation (AF) risk factors, AF symptomatology, arrhythmia recurrence rate, and readmission rate after AF catheter ablation.

NCT ID: NCT05342350 Recruiting - Clinical trials for Hepatocellular Carcinoma

International Study of High-Risk Patients for Hepatocellular Carcinoma Using Liquid Biopsy

STOP-HCC
Start date: April 15, 2022
Phase:
Study type: Observational [Patient Registry]

This study has two purposes. One is to conduct a phase IV biomarker validation study in which the investigators will prospectively survey a cohort of patients at risk for liver cancer using semi-annual abdominal ultrasound and GALAD Score for 5 years. The GALAD score is a serum biomarker-based panel that can aid in early detection among patients with a high risk for liver cancer. One is to establish a bio-repository of longitudinally collected bio-specimens from patients with fibrosis/cirrhosis as a reference set for future research.

NCT ID: NCT05354011 Recruiting - Clinical trials for Carpal Tunnel Syndrome

Effects of Kinesiotaping With and Without Active Release Technique in Patients With Carpal Tunnel Syndrome

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

The goal of this study is to compare the effects of Kinesiotaping and Active Release Technique in patients with CTS to see which method is better for improving Pain, Grip Strength, Range of Motion and functional disability.

NCT ID: NCT05356624 Recruiting - Clinical trials for De Quervain Syndrome

Mobilization With Movement Versus Soft Tissue Mobilization in Patients With De Quervain Tenosynovitis

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

this study will investigate the effects of mobilization with movement in addition to soft tissue mobilization on pain and range of motion in patients suffering from De Quervain Tenosynovitis.

NCT ID: NCT05356650 Recruiting - Clinical trials for SACROILIAC JOINT DYSFUNCTION

Mulligan's Mobilization and Proprioceptive Neuromuscular Facilitation Technique in Sacroiliac Joint Dysfunction

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

This study will aim to compare the effects of mulligan mobilization and PNF on pain and disability with patients of SIJ dysfunction and will be helpful for clinical physiotherapist to choose more effective treatment protocol for patients as there are fewer researches on comparison of these techniques.

NCT ID: NCT05356663 Recruiting - Post Operative Pain Clinical Trials

Comparative Effects of Hold Relax Technique and Mulligan Mobilization in Post Operative Knee Joint

Start date: April 15, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the comparative effects of hold relax technique and mulligan mobilization on pain, ROM and function in post operative knee joint.