NCT02395302View on ClinicalTrials.gov

Evaluation of a Dual Action Pneumatic Compression System: Tolerance and Comfort in Patients With Venous Leg Ulcers (VLUs)

NACompletedINTERVENTIONAL
Enrollment

28

Participants

Timeline

Start Date

December 31, 2014

Primary Completion Date

September 30, 2015

Study Completion Date

November 30, 2015

Conditions
Venous Leg UlcerChronic Venous InsufficiencyVenous Stasis UlcerVenous UlcerVenous Insufficiency
Interventions
DEVICE

Dual Action Pneumatic Compression

Wear in sustained mode for 14 hours and pneumatic compression mode for 3 hours during the 4 week treatment period.

Trial Locations (6)

10025

St. Luke's Roosevelt Hospital Center, New York

33125

University of Miami School Hospital, Miami

94115

Center for Clinical Research, San Francisco

02111

Tufts Medical Center, Boston

02118

Boston Medical Center, Boston

07631

Englewood Hospital and Medical Center, Englewood

Sponsors

Lead Sponsor

Tactile Medical
All Listed Sponsors
lead

Tactile Medical

INDUSTRY

NCT02395302 - Evaluation of a Dual Action Pneumatic Compression System: Tolerance and Comfort in Patients With Venous Leg Ulcers (VLUs) | Biotech Hunter | Biotech Hunter