Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01991743 · ClinicalTrials.gov registry record · NA
A Trial Comparing Combined Spinal- Epidural Dosing Strategies for External Cephalic Version
A NA study, sponsored by Northwestern University.
- Completed
- Registry status
- NA
- Development phase
- 240
- Enrollment target
NCT01991743 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 240 participants.
The verdict
NCT01991743, a NA study, has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- NA
- Development phase
- 240 participants
- Enrollment target
Study Summary
We plan to conduct a prospective, single blinded, randomized clinical trial to assess the impact of combined spinal-epidural dosing on the success rate of, and patient satisfaction during, external version for breech fetal position and the incidence of vaginal vs. Cesarean delivery. The research aim of this project is to determine the ideal neuraxial dosing strategy to maximize success of external cephalic version (ECV). The research questions, does a combined spinal-epidural (CSE) of a higher dose result in greater success in converting a breech presentation to vertex during external cephalic version (ECV). The hypotheses of this project is that CSE at higher dose will result in greater ECV success than analgesic dosing. The research significance:Increasing the success and comfort of ECV for fetal malpresentation may help decrease the cesarean section rate.
Interventions
- DRUG Group 2.5
- DRUG Group 5
- DRUG Group 7.5
- DRUG Group 10
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 240 participants |
| Start Date | 2011-05 |
| Est. Completion | 2017-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01991743
The ClinicalTrials.gov registry entry for NCT01991743 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 240 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 4 interventions - of which Group 2.5 is the first listed.
NCT01991743 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01991743 about?
NCT01991743 is a clinical study titled "A Trial Comparing Combined Spinal- Epidural Dosing Strategies for External Cephalic Version". We plan to conduct a prospective, single blinded, randomized clinical trial to assess the impact of combined spinal-epidural dosing on the success rate of, and patient satisfaction during, external version for breech fetal position and the incidence of vaginal vs. Cesarean delivery. The research ai...
What is the current status of trial NCT01991743?
This trial is currently completed. It is a NA study. The enrollment target is 240 participants. The study started on 2011-05. Estimated completion is 2017-01.
What interventions are being tested in trial NCT01991743?
The interventions under investigation include: Group 2.5 (DRUG), Group 5 (DRUG), Group 7.5 (DRUG), Group 10 (DRUG).
Who is sponsoring clinical trial NCT01991743?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.