Status:
COMPLETED
Mobius® Post-cesarean Pain Randomized Control Trial
Lead Sponsor:
Abbey Hardy-Fairbanks
Collaborating Sponsors:
Apple Medical Corporation
Conditions:
Complications; Cesarean Section
Pregnancy
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief 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 experienc...
Detailed Description
This is a prospective, randomized, patient blinded trial of standard surgical retraction versus Mobius® retraction at cesarean delivery. Women will be approached by their provider at their 36 week pre...
Eligibility Criteria
Inclusion
- Over 18 years old
- Potential for having a cesarean section (scheduled or unscheduled) at Dartmouth Hitchcock Medical Center
Exclusion
- Less than 18 years old
- Unable to consent due to language barrier or psychiatric illness
- Current methadone use for chronic pain
- Stat cesarean section
Key Trial Info
Start Date :
July 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2010
Estimated Enrollment :
154 Patients enrolled
Trial Details
Trial ID
NCT00685932
Start Date
July 1 2008
End Date
June 1 2010
Last Update
April 18 2018
Active Locations (1)
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1
Dartmouth-Hitchcock Medical Center
Lebanon, New Hampshire, United States, 03756