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Serum Antimullerian Hormone Levels in Patients Who Underwent Uterine Artery Ligation

Ovarian Reserve Clinical Trial

Official title:
Serum Antimullerian Hormone Levels in Patients Who Underwent Uterine Artery Ligation

Clinical Trial Summary

Investigators would like to see the amh values after uterine artery ligation

Clinical Trial Description

Group/cohort:

Uterine artery ligation (UAL) Investigators would like to invite the patients to the hospital at least 6 months after surgery who underwent only uterine artery ligation performed due to uterine atony during C-section.

Participants would be evaluated for their ovarian reserve via hormones and antral follicle count (AFC)

Control Group:

Investigators would like to invite the patients to the hospital at least 6 months after C-section who delivered baby without any complication.

Participants would be also evaluated for their ovarian reserve via hormones and antral follicle count (AFC) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03896243
Study type Observational
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact
Status Completed
Phase
Start date January 1, 2018
Completion date February 1, 2019
View Details
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