Status:
WITHDRAWN
Postoperative Narcotic Use After Laparoscopic Gynecologic Surgery
Lead Sponsor:
University of Tennessee, Chattanooga
Conditions:
Pelvic Pain
Endometriosis
Eligibility:
FEMALE
18-65 years
Phase:
NA
Brief Summary
This will be a prospective, randomized, double blinded placebo-controlled study at Erlanger hospital. Eligible patients who provide consent will be randomized into one of two arms receiving continuous...
Detailed Description
This will be a prospective, randomized, double blinded placebo-controlled study at Erlanger hospital. Eligible patients who provide consent will be randomized into one of two arms receiving continuous...
Eligibility Criteria
Inclusion
- All patients undergoing laparoscopic gynecologic surgery with either the traditional "straight stick" or robotic assisted techniques will be considered for eligibility. Eligible patients will include those with pelvic pain and endometriosis as well as those who present for pelvic floor reconstruction. Surgical procedures performed will include excision of endometriosis, lysis of adhesions, hysterectomy, bilateral or unilateral salpingo-oophorectomy, cystectomy, and pelvic reconstruction.
- Patients who are 18 years or older
- Patients who provide written surgical consent
- Patients who are capable and willing to follow up with surveys and complete pain and pill diaries
Exclusion
- Patients who are unable or willing to provide consent and complete the follow up surveys and dairies
- Patients who are allergic to Ropivacaine
- Patients whose minimally invasive procedures were converted to laparotomies
Key Trial Info
Start Date :
May 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 30 2020
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT04118777
Start Date
May 1 2020
End Date
July 30 2020
Last Update
July 20 2021
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