At a glance
ClinicalIndex Comparison RecordN/ACompleted· 28 enrolled
Drug / intervention
Dual Action Pneumatic Compressiondevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort in Patients With Venous Leg Ulcers
In Brief
A clinical study evaluating Dual Action Pneumatic Compression for Venous Leg Ulcer and 4 related conditions. Completed, enrolled 28 participants across 6 sites.
Detailed Summary
The purpose of the study is to assess treatment tolerance and comfort in chronic VLUs after 4 weeks of treatment using a dual action pneumatic compression device.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsVenous Leg Ulcer, Chronic Venous Insufficiency, Venous Stasis Ulcer, Venous Ulcer, Venous Insufficiency
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201520162017201820192020202120222023202420252026
Enrollment StartDec 2014
First PostedMar 2015
Primary CompletionSep 2015
Study CompletionNov 2015
TodayJul 2026
First PostedMar 23, 2015
Enrollment StartDec 1, 2014
Primary CompletionSep 1, 2015
Study CompletionNov 1, 2015
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 11.3 years ago
Interventions
Dual Action Pneumatic Compressiondevice
Wear in sustained mode for 14 hours and pneumatic compression mode for 3 hours during the 4 week treatment period.