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NCT00298571 · ClinicalTrials.gov registry record · Phase 2
Cesarean Delivery and Post-operative Pain Management With Local Anesthesia
A Phase 2 study, sponsored by University of South Florida.
- Completed
- Registry status
- Phase 2
- Development phase
- 100
- Enrollment target
NCT00298571: Completed Phase 2 study, sponsored by University of South Florida.
NCT00298571 is a Phase 2 study that has completed, run by University of South Florida. The registered enrollment target is 100 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (25% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00298571, a Phase 2 study, has completed, sponsored by University of South Florida.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 100 participants
- Enrollment target
Study Summary
The use of .5% Bupivacaine with epinephrine at the time of skin closure in cesarean deliveries will decrease post-op pain.
Interventions
- DRUG .5% bupivacaine with epinephrine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2006-02 |
| Est. Completion | 2007-10 |
| Phase | Phase 2 |
What the finished NCT00298571 record still lists
NCT00298571 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (25% lower).
The record links to 0 conditions, and to 1 intervention - of which .5% bupivacaine with epinephrine is the first listed.
NCT00298571 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00298571 about?
NCT00298571 is a clinical study titled "Cesarean Delivery and Post-operative Pain Management With Local Anesthesia". The use of .5% Bupivacaine with epinephrine at the time of skin closure in cesarean deliveries will decrease post-op pain.
What is the current status of trial NCT00298571?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2006-02. Estimated completion is 2007-10.
What interventions are being tested in trial NCT00298571?
The interventions under investigation include: .5% bupivacaine with epinephrine (DRUG).
Who is sponsoring clinical trial NCT00298571?
This trial is sponsored by University of South Florida, which has 252 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00298571's enrollment target sits among peer trials
100 672nd of 2000 higher than 1,263 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 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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