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NCT02015221 · ClinicalTrials.gov registry record · NA
Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort
A NA study, sponsored by Tactile Medical.
- Completed
- Registry status
- NA
- Development phase
- 81
- Enrollment target
NCT02015221 is a NA study that has completed, run by Tactile Medical. The registered enrollment target is 81 participants.
The verdict
NCT02015221, a NA study, has completed, sponsored by Tactile Medical.
- COMPLETED
- Registry status
- NA
- Development phase
- 81 participants
- Enrollment target
Study 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.
Interventions
- DEVICE Dual Action Pneumatic Compression Device
- DEVICE Standard Compression Garments
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 81 participants |
| Start Date | 2013-11 |
| Est. Completion | 2015-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02015221
The ClinicalTrials.gov registry entry for NCT02015221 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 81 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.
NCT02015221 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02015221 about?
NCT02015221 is a clinical study titled "Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort". 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.
What is the current status of trial NCT02015221?
This trial is currently completed. It is a NA study. The enrollment target is 81 participants. The study started on 2013-11. Estimated completion is 2015-08.
What interventions are being tested in trial NCT02015221?
The interventions under investigation include: Dual Action Pneumatic Compression Device (DEVICE), Standard Compression Garments (DEVICE).
Who is sponsoring clinical trial NCT02015221?
This trial is sponsored by Tactile Medical, which has 14 total clinical trials registered on ClinicalTrials.gov.
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