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NCT00685932 · ClinicalTrials.gov registry record · NA
Mobius® Post-cesarean Pain Randomized Control Trial
A NA study of Pregnancy and Complications; Cesarean Section, sponsored by Abbey Hardy-Fairbanks.
- Completed
- Registry status
- NA
- Development phase
- 154
- Enrollment target
- 1
- Study location
NCT00685932: Completed NA study of Pregnancy and Complications; Cesarean Section, sponsored by Abbey Hardy-Fairbanks.
NCT00685932 is a NA study of Pregnancy and Complications; Cesarean Section that has completed, run by Abbey Hardy-Fairbanks. The registered enrollment target is 154 participants, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (82% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00685932, a NA study of Pregnancy and Complications; Cesarean Section, has completed, sponsored by Abbey Hardy-Fairbanks.
- COMPLETED
- Registry status
- NA
- Development phase
- 154 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to investigate whether the use of the Mobius® retractor decreased post-operative pain after cesarean section verses conventional retractor use. Based on clinical experience and a pilot study, we suspect that the retractor will decrease overall pain as well as lateral pain.
Primary Outcome
Visual analog scale (VAS) of pain with activity on a scale of 0-15cm with 0cm: No pain to 15cm: Severe pain.
Conditions Studied
Interventions
- DEVICE Mobius Retractor
Study Locations (1)
New Hampshire
- Dartmouth-Hitchcock Medical Center - Lebanon
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 154 participants |
| Start Date | 2008-07 |
| Est. Completion | 2010-06 |
| Phase | NA |
What the finished NCT00685932 record still lists
NCT00685932 is an interventional study that assigns participants to a tested intervention. The registered 154 participants enrollment target is mid-sized for trials with a published cap, below the 872-participant average among 191 other Pregnancy trials with a reported enrollment target (82% lower).
The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 1 intervention - of which Mobius Retractor is the first listed.
NCT00685932 reports a single indexed study location in New Hampshire.
Frequently Asked Questions
What is clinical trial NCT00685932 about?
NCT00685932 is a clinical study titled "Mobius® Post-cesarean Pain Randomized Control Trial". The purpose of this study is to investigate whether the use of the Mobius® retractor decreased post-operative pain after cesarean section verses conventional retractor use. Based on clinical experience and a pilot study, we suspect that the retractor will decrease overall pain as well as lateral pai...
What is the current status of trial NCT00685932?
This trial is currently completed. It is a NA study. The enrollment target is 154 participants. The study started on 2008-07. Estimated completion is 2010-06.
What conditions does trial NCT00685932 study?
This clinical trial studies the following conditions: Pregnancy, Complications; Cesarean Section.
What interventions are being tested in trial NCT00685932?
The interventions under investigation include: Mobius Retractor (DEVICE).
Who is sponsoring clinical trial NCT00685932?
This trial is sponsored by Abbey Hardy-Fairbanks, which has 2 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00685932 being conducted?
This trial has 1 study location across New Hampshire. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT00685932's enrollment target sits among peer trials
154 95th of 191 higher than 97 of 191 other Pregnancy trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Pregnancy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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