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NCT02008591 · ClinicalTrials.gov registry record · Phase 4
Comparison of Epidural Labor Pain Relief Techniques on Maternal and Fetal Outcomes
A Phase 4 study of Laboring Women Requesting Neuraxial Labor Analgesia, sponsored by Brigham and Women's Hospital.
- Completed
- Registry status
- Phase 4
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT02008591 is a Phase 4 study of Laboring Women Requesting Neuraxial Labor Analgesia that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 120 participants. The trial reports 1 study location across 1 state.
The verdict
NCT02008591, a Phase 4 study of Laboring Women Requesting Neuraxial Labor Analgesia, has completed, sponsored by Brigham and Women's Hospital.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary objective of this study is to compare the onset and duration of the initial dose of medications given through three different epidural (conventional epidural, combined spinal epidural and dural puncture epidural) techniques for labor pain relief. The secondary objective of this study is to compare the fetal effects of these three epidural labor analgesia techniques.
Conditions Studied
Interventions
- PROCEDURE Epidural Technique versus Dural Puncture Epidural Technique versus Combined Spinal Epidural Technique
Study Locations (1)
Massachusetts
- Brigham and Women's Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2013-11-26 |
| Est. Completion | 2016-01-27 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02008591
The ClinicalTrials.gov registry entry for NCT02008591 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Brigham and Women's Hospital, which has 937 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Laboring Women Requesting Neuraxial Labor Analgesia appearing as the primary indexed condition, and to 1 intervention - of which Epidural Technique versus Dural Puncture Epidural Technique versus Combined Spinal Epidural Technique is the first listed.
NCT02008591 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT02008591 about?
NCT02008591 is a clinical study titled "Comparison of Epidural Labor Pain Relief Techniques on Maternal and Fetal Outcomes". The primary objective of this study is to compare the onset and duration of the initial dose of medications given through three different epidural (conventional epidural, combined spinal epidural and dural puncture epidural) techniques for labor pain relief. The secondary objective of this study is...
What is the current status of trial NCT02008591?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2013-11-26. Estimated completion is 2016-01-27.
What conditions does trial NCT02008591 study?
This clinical trial studies the following conditions: Laboring Women Requesting Neuraxial Labor Analgesia.
What interventions are being tested in trial NCT02008591?
The interventions under investigation include: Epidural Technique versus Dural Puncture Epidural Technique versus Combined Spinal Epidural Technique (PROCEDURE).
Who is sponsoring clinical trial NCT02008591?
This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02008591 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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