Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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: Completed NA study, sponsored by Hospital for Special Surgery, New York.

NCT02345642 is a NA study that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 20 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

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.

Primary Outcome

Ultrasound of the venous system just below the saphenofemoral junction to assess the venous velocity will be taken before and after application the VenaFlow and the ActiveCare+S.F.T pneumatic compression devices. Change from Baseline in Peak Venous Velocity 30 minutes after Device is applied is recorded.

Interventions

  • DEVICE ActiveCare+SFT Supine
  • DEVICE VenaFlow Elite Supine
  • DEVICE ActiveCare+SFT Standing
  • DEVICE VenaFlow Elite Standing

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2015-02
Est. Completion 2016-01
Phase NA

What the finished NCT02345642 record still lists

NCT02345642 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 4 interventions - of which ActiveCare+SFT Supine is the first listed.

NCT02345642 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT02345642's enrollment target sits among peer trials

20 1768th of 2000 higher than 140 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02345642, the US trial registry maintained by the National Library of Medicine. NCT02345642 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.