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NCT01750099 · ClinicalTrials.gov registry record · NA
Pain Relief Effects on Length of Labor
A NA study, sponsored by University of Texas Southwestern Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 202
- Enrollment target
NCT01750099 is a NA study that has completed, run by University of Texas Southwestern Medical Center. The registered enrollment target is 202 participants.
The verdict
NCT01750099, a NA study, has completed, sponsored by University of Texas Southwestern Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 202 participants
- Enrollment target
Study Summary
This study divides patients into two groups when they ask for medicine to help relieve the pain of contractions. One group will be selected to receive an epidural and another group will be selected to receive both a spinal dose and an epidural. The investigators will then measure how long it takes to deliver the baby. The investigators think that the group that has the combination spinal and epidural will have a faster labor.
Interventions
- PROCEDURE Combined Spinal-epidural
- PROCEDURE Continuous Lumbar epidural
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 202 participants |
| Start Date | 2013-02 |
| Est. Completion | 2014-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01750099
The ClinicalTrials.gov registry entry for NCT01750099 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 202 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Texas Southwestern Medical Center, which has 837 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Combined Spinal-epidural is the first listed.
NCT01750099 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01750099 about?
NCT01750099 is a clinical study titled "Pain Relief Effects on Length of Labor". This study divides patients into two groups when they ask for medicine to help relieve the pain of contractions. One group will be selected to receive an epidural and another group will be selected to receive both a spinal dose and an epidural. The investigators will then measure how long it takes t...
What is the current status of trial NCT01750099?
This trial is currently completed. It is a NA study. The enrollment target is 202 participants. The study started on 2013-02. Estimated completion is 2014-05.
What interventions are being tested in trial NCT01750099?
The interventions under investigation include: Combined Spinal-epidural (PROCEDURE), Continuous Lumbar epidural (PROCEDURE).
Who is sponsoring clinical trial NCT01750099?
This trial is sponsored by University of Texas Southwestern Medical Center, which has 837 total clinical trials registered on ClinicalTrials.gov.
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