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NCT00356434 · ClinicalTrials.gov registry record · NA
A Comparison of Sequential Compression Devices and Foot Pumps in the Obstetric Population
A NA study, sponsored by Johns Hopkins University.
- Terminated
- Registry status
- NA
- Development phase
- 11
- Enrollment target
NCT00356434: Clinical Trial NA study, sponsored by Johns Hopkins University.
NCT00356434 is a NA study that was terminated before completion, run by Johns Hopkins University. The registered enrollment target is 11 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.
The verdict
NCT00356434, a NA study, was terminated before completion, sponsored by Johns Hopkins University.
- TERMINATED
- Registry status
- NA
- Development phase
- 11 participants
- Enrollment target
Study Summary
The researchers at Johns Hopkins University believe that the foot pump will be superior to sequential compression devices in comfort and patient compliance which may increase provider efforts to prevent deep vein thrombosis (DVT) in pregnancy.
Primary Outcome
Scale of 1-10 (1 being very uncomfortable and 10 being very uncomfortable) describing level of comfort during the time of device use (composite score of heat, softness, discomfort).
Interventions
- DEVICE Kendall A-V foot impulse pump, model 6060
- DEVICE Kendall sequential compression device, model 9525
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2008-11 |
| Est. Completion | 2009-12 |
| Phase | NA |
Why NCT00356434 stopped before completion
NCT00356434 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 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 2 interventions - of which Kendall A-V foot impulse pump, model 6060 is the first listed.
NCT00356434 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00356434 about?
NCT00356434 is a clinical study titled "A Comparison of Sequential Compression Devices and Foot Pumps in the Obstetric Population". The researchers at Johns Hopkins University believe that the foot pump will be superior to sequential compression devices in comfort and patient compliance which may increase provider efforts to prevent deep vein thrombosis (DVT) in pregnancy.
What is the current status of trial NCT00356434?
This trial is currently terminated. It is a NA study. The enrollment target is 11 participants. The study started on 2008-11. Estimated completion is 2009-12.
What interventions are being tested in trial NCT00356434?
The interventions under investigation include: Kendall A-V foot impulse pump, model 6060 (DEVICE), Kendall sequential compression device, model 9525 (DEVICE).
Who is sponsoring clinical trial NCT00356434?
This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00356434's enrollment target sits among peer trials
11 1927th of 2000 higher than 74 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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