CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 21 enrolled
Drug / intervention
pneumatic compression - 1 hour per day +2 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/NCT02031627
NCT02031627N/ACompleted
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Physiologic Response to Varying Lymphoedema Compression Programs With the Flexitouch System

Tactile Medical·interventional·Posted Jan 9, 2014·Updated Jul 20, 2021

In Brief

A clinical study evaluating pneumatic compression - 1 hour per day, pneumatic compression - 2 hours per day, and 1 other intervention for Lower Extremity Lymphoedema and Leg Lymphoedema. Completed, enrolled 21 participants across 1 site.

Detailed Summary

Proof of principle study in order to determine if there is a difference in treatment effect across the 3 study groups when treating lower extremity lymphoedema using a pneumatic compression device.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLower Extremity Lymphoedema, Leg Lymphoedema
CountriesUnited Kingdom
Collaborators--

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJan 9, 2014
Enrollment StartNov 11, 2013
Primary CompletionMar 31, 2019
Study CompletionJun 30, 2019
TodayJul 2, 2026
Enrollment to primary: 5.4 yearsPosted 12.5 years ago

Interventions

pneumatic compression - 1 hour per daydevice

Pneumatic compression treatment once per day (1 hour)

pneumatic compression - 2 hours per daydevice

pneumatic compression treatment twice per day in the AM \& PM (2 hours)

pneumatic compression - 4 hours per daydevice

pneumatic compression treatment twice per day consisting of 2 consecutive 1 hour treatments in the AM \& PM (4 hours)