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NCT00380978 · ClinicalTrials.gov registry record · NA
Neuraxial Versus Systemic Analgesia for Latent Phase Labor Effect on Rate of Operative Delivery
A NA study, sponsored by Northwestern University.
- Completed
- Registry status
- NA
- Development phase
- 1,026
- Enrollment target
NCT00380978 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 1,026 participants.
The verdict
NCT00380978, a NA study, has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,026 participants
- Enrollment target
Study Summary
The purpose of this study in nulliparous women undergoing induction of labor is to determine whether initiation of neuraxial analgesia compared to systemic opioid analgesia early in labor (\< 4 cm cervical dilation)affects the cesarean delivery rate.
Interventions
- PROCEDURE combined spinal epidural analgesia
- PROCEDURE late analgesia (systemic)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,026 participants |
| Start Date | 2001-10 |
| Est. Completion | 2008-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00380978
The ClinicalTrials.gov registry entry for NCT00380978 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,026 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which combined spinal epidural analgesia is the first listed.
NCT00380978 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00380978 about?
NCT00380978 is a clinical study titled "Neuraxial Versus Systemic Analgesia for Latent Phase Labor Effect on Rate of Operative Delivery". The purpose of this study in nulliparous women undergoing induction of labor is to determine whether initiation of neuraxial analgesia compared to systemic opioid analgesia early in labor (\< 4 cm cervical dilation)affects the cesarean delivery rate.
What is the current status of trial NCT00380978?
This trial is currently completed. It is a NA study. The enrollment target is 1,026 participants. The study started on 2001-10. Estimated completion is 2008-09.
What interventions are being tested in trial NCT00380978?
The interventions under investigation include: combined spinal epidural analgesia (PROCEDURE), late analgesia (systemic) (PROCEDURE).
Who is sponsoring clinical trial NCT00380978?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
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