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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Bilateral salpingectomy | Surgical bilateral removal of fallopian tubes (not involving ovaries) |
| PROCEDURE | Tubal ligation | Bilateral 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.