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NCT01062893 · ClinicalTrials.gov registry record · Phase 2
Combined Spinal/Epidural (CSE) Saline Duration/Spread
A Phase 2 study, sponsored by Wake Forest University Health Sciences.
- Terminated
- Registry status
- Phase 2
- Development phase
- 82
- Enrollment target
NCT01062893 is a Phase 2 study that was terminated before completion, run by Wake Forest University Health Sciences. The registered enrollment target is 82 participants.
The verdict
NCT01062893, a Phase 2 study, was terminated before completion, sponsored by Wake Forest University Health Sciences.
- TERMINATED
- Registry status
- Phase 2
- Development phase
- 82 participants
- Enrollment target
Study Summary
An attempt is being made to see if by injecting a set volume of sterile saline into the epidural space during the treatment of labor pain with a combined spinal/epidural (CSE) increases the amount of pain relief obtained and makes the labor analgesia lasts longer. Subjects are in the study from the time their CSE is placed until they request additional pain medication from the spinal dose of numbing medicine wearing off.
Interventions
- OTHER Sterile normal saline 0 mls
- OTHER 15 mls sterile normal saline
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 82 participants |
| Start Date | 2009-08 |
| Est. Completion | 2012-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01062893
The ClinicalTrials.gov registry entry for NCT01062893 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 82 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Sterile normal saline 0 mls is the first listed.
NCT01062893 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01062893 about?
NCT01062893 is a clinical study titled "Combined Spinal/Epidural (CSE) Saline Duration/Spread". An attempt is being made to see if by injecting a set volume of sterile saline into the epidural space during the treatment of labor pain with a combined spinal/epidural (CSE) increases the amount of pain relief obtained and makes the labor analgesia lasts longer. Subjects are in the study from the ...
What is the current status of trial NCT01062893?
This trial is currently terminated. It is a Phase 2 study. The enrollment target is 82 participants. The study started on 2009-08. Estimated completion is 2012-09.
What interventions are being tested in trial NCT01062893?
The interventions under investigation include: Sterile normal saline 0 mls (OTHER), 15 mls sterile normal saline (OTHER).
Who is sponsoring clinical trial NCT01062893?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
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