CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 81 enrolled
Drug / intervention
Dual Action Pneumatic Compression Device +1 moredevice
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.

Search/NCT02015221
NCT02015221N/ACompleted

Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort

Tactile Medical·interventional·Posted Dec 19, 2013·Updated Dec 15, 2016

In Brief

A clinical study evaluating Dual Action Pneumatic Compression Device and Standard Compression Garments for Chronic Venous Insufficiency. Completed, enrolled 81 participants across 11 sites.

Detailed Summary

The purpose of this study is to determine the ease of use and comfort of the ACTitouch dual action pneumatic compression device in patients with unilateral or bilateral chronic venous insufficiency (CVI) with or without venous leg ulcers, as compared to standard compression.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedDec 19, 2013
Enrollment StartNov 1, 2013
Primary CompletionJul 1, 2015
Study CompletionAug 1, 2015
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 12.5 years ago

Interventions

Dual Action Pneumatic Compression Devicedevice

A novel dual action pneumatic compression device that provides both sustained compression while ambulatory, and intermittent pneumatic compression when connected to an AC outlet.

Standard Compression Garmentsdevice

Compression stockings with a 30-40mmHg level of compression.