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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 is a Phase 4 study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 127 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00151346
The ClinicalTrials.gov registry entry for NCT00151346 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 127 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Bupivacaine and Fentanyl (for CSE) is the first listed.
NCT00151346 reports 0 study locations.
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.
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