Status:
COMPLETED
Fascial Closure Technique After Gynecologic Laparoscopic Surgery and Postoperative Pain
Lead Sponsor:
Jessica G Putman
Conditions:
Pain, Postoperative
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
Our study aims to determine postoperative pain outcomes when comparing port site \> 10 mm fascial closure with traditional direct closure versus use of laparoscopic fascial closure device in patients ...
Eligibility Criteria
Inclusion
- Patients aged 18 or older.
- Any patient undergoing laparoscopic gynecologic surgery with one left upper quadrant port site \> 10 mm via either robotic or traditional laparoscopic techniques for any indication including abnormal bleeding, pelvic pain, gynecologic cancer, uterine fibroids, etc. Procedures performed will include but not be limited to hysterectomy, bilateral or unilateral salpingoophorectomy, ovarian cystectomy, and pelvic floor support procedures.
- Patients willing and able to give informed consent.
- Patients capable and willing to return for follow up and complete pain diaries.
Exclusion
- Patients unable to return for follow up.
- Patients undergoing laparoscopic surgery that requires conversion to laparotomy.
- Patients undergoing laparoscopic surgery that does not require a port site \>10 mm.
Key Trial Info
Start Date :
March 5 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 14 2022
Estimated Enrollment :
123 Patients enrolled
Trial Details
Trial ID
NCT04765306
Start Date
March 5 2021
End Date
April 14 2022
Last Update
May 12 2022
Active Locations (1)
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1
Erlanger Baroness Hospital
Chattanooga, Tennessee, United States, 37403