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Compression; Vein clinical trials

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NCT ID: NCT06438133 Not yet recruiting - Clinical trials for Venous Insufficiency

Digital Supported Compression Bandaging in Patients With Chronic Edema in the Lower Limbs

CIMON
Start date: June 2024
Phase:
Study type: Observational

Patients with chronic edema of the lower limb referred to compression bandaging in a hospital setting will be invited to participate in the validation study of a novel sensor (CIMON), which have been developed for assessing the effect of compression bandaging. Participants will have the sensor applied to the lower limb before initiation of compression bandaging and will receive usual compression treatment according to severity of the edema and usual practice at the treatment site. Duration of participation is 14 days.

NCT ID: NCT05212363 Terminated - Sedentary Behavior Clinical Trials

Lower Leg Compression in Extended Video Game Play: A Pilot Study

Start date: December 9, 2021
Phase: N/A
Study type: Interventional

Compression garments are used to exert external pressure on the lower extremities to reduce vascular wall tension and prevent gravity form pooling blood in the lower extremities which will improve venous return and lymphatic output. Given the nature of video game play, sitting for prolonged periods of time without an active break is the perfect scenario to put these players at risk for deep vein thromboses (DVTs). Graduated compression wear may offer significant health benefits to this rapidly expanding sport. This study is essential to the formation of effective performance wear to reduce health risks in a gaming population.

NCT ID: NCT04837560 Recruiting - Edema Leg Clinical Trials

Safety and Efficacy of the ElastiMed's SACS 2.0 - Smart Active Compression Stocking for the Treatment of Venous Edema

Start date: April 2021
Phase: Phase 1
Study type: Interventional

Device Efficacy: The primary efficacy assessment will be defined as successful if the edema volume will be reduced over time after using the SACS 2.0 device. Treatment and edema evaluation will be performed in comparison to a standard compression bandage. The treatment will be performed for several hours during the subject's daily rest time. The Measurements will be performed daily before treatment initiation and without the device on the leg (baseline) (T0); and after four hours of device operation. The edema volume will be measured by a calf circumference measurement.

NCT ID: NCT04096729 Completed - Clinical trials for Patient Satisfaction

Patients Commitment to Compression Therapy

POMP
Start date: October 1, 2019
Phase:
Study type: Observational

The study Patients Commitment to compression therapy (POMP) is observational, prospective. After the Phlebologist consultation after 1 month and 1 year, a telephone questionnaire is carried out for the patients included in the study with the involvement of a company specializing in conducting a telephone questionnaire. Patients will be interviewed about the implementation of the doctor's recommendations regarding compression therapy over a period 1 month and 1 year.

NCT ID: NCT03725111 Completed - Leg Ulcer Clinical Trials

Haemodynamics Variations of Transcutaneous Oxygen in Patient With Areterio-venous Leg Ulcers Under Venous Compression

Start date: December 30, 2018
Phase: N/A
Study type: Interventional

Arterio-venous leg ulcers are real problems when it comes to public health because it has a major cost and leads to social and professional handicap. The management of leg ulcers is not clear and can be venous compression or surgery. The aim of the study is to evaluate the variation of the transcutaneous oxygen with compression. The second aim is to see how tolerate is the compression and the quality of life.

NCT ID: NCT03330925 Completed - Compression; Vein Clinical Trials

Safety and Feasibility of the ElastiMed's SACS

Start date: January 24, 2018
Phase: N/A
Study type: Interventional

The main objective of this study is to demonstrate the safety and the feasibility of this device, and its ability to increase venous blood flow Primary safety Endpoint: To demonstrate the safety of the device- no serious adverse effect Primary feasibility Endpoint: Increase the blood flow velocity The blood flow will be detected by a Duplex Ultrasonography test at the popliteal vein and the femoral vein. The volunteers will rest at controlled environment room . Measurements will be performed after 30 min of rest without the device on the leg (baseline) and after 30 min of device activity .