N/A
N=154
Mobius® Post-cesarean Pain Randomized Control Trial
Complications; Cesarean Section · Pregnancy
Bottom Line
View on ClinicalTrials.gov: NCT00685932 ↗Enrolled (actual)
154
Serious AEs
0.0%
Results posted
Apr 2018
Primary outcome: Primary: The Degree of Pain With Activity on Post-operative Day Number Two — 6.4; 6.3 cm
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Mobius Retractor (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- Female
- Sponsor
- Abbey Hardy-Fairbanks
- Primary completion
- Jun 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Degree of Pain With Activity on Post-operative Day Number Two |
6.4; 6.3 | — |
| SECONDARY Number of Participants Who Report Asymmetrical Pain on Second Post-operative Day After Cesarean Delivery |
33; 32 | — |
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.
Eligibility Criteria
Inclusion Criteria
- Over 18 years old
- Potential for having a cesarean section (scheduled or unscheduled) at Dartmouth Hitchcock Medical Center
Exclusion Criteria
- Less than 18 years old
- Unable to consent due to language barrier or psychiatric illness
- Current methadone use for chronic pain
- Stat cesarean section
Data sourced from ClinicalTrials.gov (NCT00685932). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.