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NCT02680834 · ClinicalTrials.gov registry record · NA

VLU Non-Inferiority Study Comparing a Dual Action Pneumatic Compression Device to Multi-Layer Bandaging

A NA study, sponsored by Tactile Medical.

Terminated
Registry status
NA
Development phase
56
Enrollment target

NCT02680834: Clinical Trial NA study, sponsored by Tactile Medical.

NCT02680834 is a NA study that was terminated before completion, run by Tactile Medical. The registered enrollment target is 56 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02680834, a NA study, was terminated before completion, sponsored by Tactile Medical.

TERMINATED
Registry status
NA
Development phase
56 participants
Enrollment target

Study Summary

The purpose of the study is to test non-inferiority of chronic Venous Leg Ulcer (VLU) area reduction at 16 weeks with a dual action pneumatic compression device compared to multi-layer bandaging.

Primary Outcome

Percentage of ulcer area reduction in the target VLU during the 16 week treatment period calculated by wound imaging software.

Interventions

  • DEVICE Dual Action Pneumatic Compression Device
  • DEVICE Multi-Layer Bandaging

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2016-02
Est. Completion 2017-06
Phase NA
Tactile Medical

14 total trials

Why NCT02680834 stopped before completion

NCT02680834 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Dual Action Pneumatic Compression Device is the first listed.

NCT02680834 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02680834 about?

NCT02680834 is a clinical study titled "VLU Non-Inferiority Study Comparing a Dual Action Pneumatic Compression Device to Multi-Layer Bandaging". The purpose of the study is to test non-inferiority of chronic Venous Leg Ulcer (VLU) area reduction at 16 weeks with a dual action pneumatic compression device compared to multi-layer bandaging.

What is the current status of trial NCT02680834?

This trial is currently terminated. It is a NA study. The enrollment target is 56 participants. The study started on 2016-02. Estimated completion is 2017-06.

What interventions are being tested in trial NCT02680834?

The interventions under investigation include: Dual Action Pneumatic Compression Device (DEVICE), Multi-Layer Bandaging (DEVICE).

Who is sponsoring clinical trial NCT02680834?

This trial is sponsored by Tactile Medical, which has 14 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02680834's enrollment target sits among peer trials

56 1262nd of 2000 higher than 737 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02680834, the US trial registry maintained by the National Library of Medicine. NCT02680834 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.