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NCT02345642 · ClinicalTrials.gov registry record · NA
A Hemodynamic Comparison of Stationary and Portable Pneumatic Compression Devices
A NA study, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT02345642 is a NA study that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 20 participants.
The verdict
NCT02345642, a NA study, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
We are comparing two pneumatic compression devices, VenaFlow (stationary) and MCS (portable) in both the supine an standing position. We will start supine and will take 3 baseline measurements of venous velocity and then apply a device and take 3 measurements of the increase in peak venous velocity. We will repeat this with the second device. We will then have the subject stand and repeat the above with each device. We will randomize the order of the devices in the supine and standing position. This study will involve 10 healthy subjects of various ages and 10 total hip replacements (THR) patients.
Interventions
- DEVICE ActiveCare+SFT Supine
- DEVICE VenaFlow Elite Supine
- DEVICE ActiveCare+SFT Standing
- DEVICE VenaFlow Elite Standing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2015-02 |
| Est. Completion | 2016-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02345642
The ClinicalTrials.gov registry entry for NCT02345642 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hospital for Special Surgery, New York, which has 194 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 4 interventions - of which ActiveCare+SFT Supine is the first listed.
NCT02345642 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02345642 about?
NCT02345642 is a clinical study titled "A Hemodynamic Comparison of Stationary and Portable Pneumatic Compression Devices". We are comparing two pneumatic compression devices, VenaFlow (stationary) and MCS (portable) in both the supine an standing position. We will start supine and will take 3 baseline measurements of venous velocity and then apply a device and take 3 measurements of the increase in peak venous velocity....
What is the current status of trial NCT02345642?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2015-02. Estimated completion is 2016-01.
What interventions are being tested in trial NCT02345642?
The interventions under investigation include: ActiveCare+SFT Supine (DEVICE), VenaFlow Elite Supine (DEVICE), ActiveCare+SFT Standing (DEVICE), VenaFlow Elite Standing (DEVICE).
Who is sponsoring clinical trial NCT02345642?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
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