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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. 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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00356434
The ClinicalTrials.gov registry entry for NCT00356434 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.
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 reports 0 study locations.
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.
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