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Serum Antimullerian Hormone Levels in Patients Who Underwent Uterine Artery Ligation

N/ACompletedNCT03896243
Kanuni Sultan Suleyman Training and Research Hospital102 enrolled

Overview

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

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 Type

OBSERVATIONAL

Enrollment

102

Conditions

Uterine Artery LigationOvarian Reserve

Interventions

Uterine artery ligation (UAL)DIAGNOSTIC_TEST

Uterine artery ligation (UAL) We will 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. They will evaluated for their ovarian reserve via hormones and antral follicle count (AFC)

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 35 YearsHealthy volunteers:
Medical Language ↔ Plain English
Inclusion Criteria: * age 18- 35 years * no systemic or endocrine diseases * patients who had uterine artery ligation due to atony * healthy postpartum patients as controls Exclusion Criteria: * patients with PCOS * Pregnancy with IVF or oosit donation * Patients with endocrinopathy, diseases which require radiotherapy and chemotherapy etc. * Patients with BMI \>40

Locations (1)

Pinar Yalcin Bahat

Istanbul, İ̇stanbul, Turkey (Türkiye)

Outcomes

Primary Outcomes

1.ovarian reserve in patients with uterine artery ligation

calculation of ovarian reserve with amh (ng/ml) after uterine artery ligation due to uterine atony

Time frame: 12 months

Data from ClinicalTrials.gov

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