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NCT04750486 · ClinicalTrials.gov registry record · NA
Lower Limb Compression Prevents Hypotension After Epidural in Labor
A NA study, sponsored by Wayne State University.
- Completed
- Registry status
- NA
- Development phase
- 240
- Enrollment target
NCT04750486: Completed NA study, sponsored by Wayne State University.
NCT04750486 is a NA study that has completed, run by Wayne State University. The registered enrollment target is 240 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04750486, a NA study, has completed, sponsored by Wayne State University.
- COMPLETED
- Registry status
- NA
- Development phase
- 240 participants
- Enrollment target
Study Summary
The goal of this study is to determine whether the use of sequential compression devices (lower limb compression) can reduce the rate of maternal hypotension after epidural, and therefore reduce the incidence of fetal heart tracing complications during labor.
Primary Outcome
Determined by maternal blood pressure measurements.
Interventions
- DEVICE Sequential compression devices
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 240 participants |
| Start Date | 2021-02-05 |
| Est. Completion | 2023-02-15 |
| Phase | NA |
What the finished NCT04750486 record still lists
NCT04750486 is an interventional study that assigns participants to a tested intervention. The registered 240 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (83% lower).
The record links to 0 conditions, and to 1 intervention - of which Sequential compression devices is the first listed.
NCT04750486 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04750486 about?
NCT04750486 is a clinical study titled "Lower Limb Compression Prevents Hypotension After Epidural in Labor". The goal of this study is to determine whether the use of sequential compression devices (lower limb compression) can reduce the rate of maternal hypotension after epidural, and therefore reduce the incidence of fetal heart tracing complications during labor.
What is the current status of trial NCT04750486?
This trial is currently completed. It is a NA study. The enrollment target is 240 participants. The study started on 2021-02-05. Estimated completion is 2023-02-15.
What interventions are being tested in trial NCT04750486?
The interventions under investigation include: Sequential compression devices (DEVICE).
Who is sponsoring clinical trial NCT04750486?
This trial is sponsored by Wayne State University, which has 163 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04750486's enrollment target sits among peer trials
240 440th of 2000 higher than 1,542 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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