The objective of this study is to evaluate the feasibility and safety of salpingectomy versus standard tubal ligation in women undergoing surgical sterilization at the time of a planned cesarean delivery. Salpingectomy is currently being investigated as a potential strategy for ovarian cancer prevention. While this procedure is currently performed during hysterectomies, its feasibility at the time of cesarean delivery is not well established. This randomized, prospective clinical trial will compare the two sterilization methods to demonstrate that salpingectomy compared with standard tubal ligation at the time of cesarean delivery will not result in increased operative time, blood loss or other complications. This study is necessary to promote salpingectomy as a standard sterilization method during cesarean deliveries.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
44
Bilateral salpingectomy will be performed instead of standard tubal ligation as sterilization during cesarean section.
Standard tubal ligation by either Parkland or Pomeroy technique will be performed at cesarean section
University of Virginia
Charlottesville, Virginia, United States
Time of tubal ligation
Primary outcome will be the time it takes to complete the sterilization procedure
Time frame: at time of procedure
Total procedure time
The total time it takes to complete the cesarean plus sterilization procedure
Time frame: at time of procedure
Estimated blood loss
Estimated blood loss for the entire procedure
Time frame: at time of procedure
Rate of aborted procedures
Inability to complete bilateral salpingectomy in the experimental arm
Time frame: at time of procedure
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