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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 is a NA study that was terminated before completion, run by Tactile Medical. The registered enrollment target is 56 participants.
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.
Interventions
- DEVICE Dual Action Pneumatic Compression Device
- DEVICE Multi-Layer Bandaging
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 56 participants |
| Start Date | 2016-02 |
| Est. Completion | 2017-06 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02680834
The ClinicalTrials.gov registry entry for NCT02680834 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 56 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tactile Medical, which has 14 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Dual Action Pneumatic Compression Device is the first listed.
NCT02680834 reports 0 study locations.
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.
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