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NCT00151346 · ClinicalTrials.gov registry record · Phase 4
Combined Spinal-Epidural Versus Traditional Labor Epidural
A Phase 4 study, sponsored by Weill Medical College of Cornell University.
- Completed
- Registry status
- Phase 4
- Development phase
- 127
- Enrollment target
NCT00151346: Completed Phase 4 study, sponsored by Weill Medical College of Cornell University.
NCT00151346 is a Phase 4 study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 127 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (75% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00151346, a Phase 4 study, has completed, sponsored by Weill Medical College of Cornell University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 127 participants
- Enrollment target
Study Summary
The purpose of this study to compare the use of spinal-epidural versus traditional labor epidural on maternal and fetal effects. The hope is to determine the safest and most effective epidural method of relieving pain during labor.
Interventions
- DRUG Bupivacaine and Fentanyl (for CSE)
- DRUG Bupivacaine and Fentanyl (for traditional epidural)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 127 participants |
| Start Date | 2003-10 |
| Est. Completion | 2006-09 |
| Phase | Phase 4 |
What the finished NCT00151346 record still lists
NCT00151346 is an interventional study that assigns participants to a tested intervention. The registered 127 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (75% lower).
The record links to 0 conditions, and to 2 interventions - of which Bupivacaine and Fentanyl (for CSE) is the first listed.
NCT00151346 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00151346 about?
NCT00151346 is a clinical study titled "Combined Spinal-Epidural Versus Traditional Labor Epidural". The purpose of this study to compare the use of spinal-epidural versus traditional labor epidural on maternal and fetal effects. The hope is to determine the safest and most effective epidural method of relieving pain during labor.
What is the current status of trial NCT00151346?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 127 participants. The study started on 2003-10. Estimated completion is 2006-09.
What interventions are being tested in trial NCT00151346?
The interventions under investigation include: Bupivacaine and Fentanyl (for CSE) (DRUG), Bupivacaine and Fentanyl (for traditional epidural) (DRUG).
Who is sponsoring clinical trial NCT00151346?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00151346's enrollment target sits among peer trials
127 639th of 2000 higher than 1,355 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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