Status:
COMPLETED
Single Port Insufflation RCT
Lead Sponsor:
University of Chicago
Conditions:
Postoperative Pain Score
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The goal of this clinical trial is to learn if decreasing insufflation pressure during minimally invasive single port robotic sacrocolpopexy improved postoperative pain without impacting surgeon intra...
Detailed Description
This was a double-blinded, randomized control trial of women undergoing single port robotic sacrocolpopexy with intraperitoneal insufflation pressure set to 15 mm Hg (standard pressure) or 12 mm Hg (e...
Eligibility Criteria
Inclusion
- Adult women scheduled for single port robotic sacrocolpopexy for uterovaginal or vaginal vault prolapse
Exclusion
- Non-english speaking
- Inability to complete study questionnaires
Key Trial Info
Start Date :
April 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2025
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT06990750
Start Date
April 1 2024
End Date
April 1 2025
Last Update
May 25 2025
Active Locations (1)
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1
The University of Chicago
Chicago, Illinois, United States, 60637