Clinical Trials Directory

Trials / Unknown

UnknownNCT02377128

Ovarian Reserve Following Bilateral Salpingectomy Versus Tubal Ligation During Cesarean Section

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
45 (estimated)
Sponsor
Wolfson Medical Center · Other Government
Sex
Female
Age
Healthy volunteers
Accepted

Summary

The aforementioned study was designed to evaluate short term ovarian reserve as assessed by anti-Mullerian hormone(AMH) levels following bilateral salpingectomy versus tubal ligation, as part of cesarean sections performed in women requesting future sterilization. The investigators aim to recruit 3 groups of 15 women undergoing elective cesarean section at the investigators' institution, 2 of which request sterilization (allocated to tubal ligation or bilateral salpingectomy) and one undergoing solely cesarean section. The groups will have blood drawn for AMH prior to the procedure and at a post-operation visit 8 weeks following. This is preformed in light of validated data offering better sterilization and possible diminished future risk of ovarian cancer with salpingectomy. Also, is has been proved to be just as safe as tubal ligation. This will be performed as a randomized controlled trial.

Conditions

Interventions

TypeNameDescription
PROCEDUREBilateral salpingectomySurgical bilateral removal of fallopian tubes (not involving ovaries)
PROCEDURETubal ligationBilateral ligation of fallopian tubes (not involving ovaries)

Timeline

Start date
2015-03-01
Primary completion
2016-12-01
First posted
2015-03-03
Last updated
2016-04-29

Source: ClinicalTrials.gov record NCT02377128. Inclusion in this directory is not an endorsement.