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Clinical Trial Summary

The objective of this Bayesian Adaptive trial is to compare a control group versus a comprehensive ulcer healing protocol. The latter involves a combination of compressive therapy, miokinetic drainage and muscle strengthening for the entire lower extremity pump among patients with lower extremity venous ulcers. The investigators hypothesized that the combined therapy will have a higher closure rate as well as lower time to closure.


Clinical Trial Description

This is a Bayesian adaptive, randomized, controlled, parallel, two-armed Bayesian adaptive trial. Patients diagnosed with varicose ulcers through Doppler ultrasonography will be recruited at the Pro Circulation Clinic of Angiology and Vascular Surgery, Brazil. The active group will be the Vein Fitness system, a multimodal intervention comprising exercise, lymphatic drainage, and compressive therapy, while the control group will be standard compressive therapy and regular wound care. The researchers will measure closure of the wounds and the closure rate as the primary outcomes. The study was designed in accordance with the CONSORT statement. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03127904
Study type Interventional
Source Pró Circulação®
Contact Eduardo Matta, MD
Phone 55 (49) 3433-9050
Email procirculacao@gmail.com
Status Recruiting
Phase N/A
Start date July 24, 2018
Completion date December 30, 2025

See also
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