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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02995343
Other study ID # 2.100.2014.0076
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 2016
Est. completion date September 2019

Study information

Verified date March 2019
Source Ege University
Contact cagdas sahin, MD
Phone +905324676106
Email cagdasdr@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients who hypogastric arteries and/or uterine arteries had been ligated will be evaluated in terms of ovarian reserve markers such as anti-mullerian hormone levels, ovarian volumes, antral follicule count, follicule stimuli hormone and estrogen levels. Investigators will search their archives for finding suitable patients for study. Investigators will especially notice being at least 6 month time of interval between surgery and evaluation time. Ultrasound examination and taking blood sample will be performed on 2nd or 3th day of menstrual cycle. These results will be compared with normal postpartum women's results. It will be evaluated that there is or not any effect of the hypogastric arteries and/or uterine arteries on ovarian reserve


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date September 2019
Est. primary completion date August 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Patients had been ligated hypogastric and/or uterine arteries

- Patients are in 6 month period after surgery

- Without performed hysterectomy

- No older than 40 years old

- No history about endocrinopathy which have an effect upon ovarian reserve

Exclusion Criteria:

- Patients had been made other gynecologic surgery such as fallopian tube ligation and hysterectomy etc.

- Patients are older than 40 years old

- Patients use drugs which have an effect upon ovarian reserve

- Patients have diseases which have an effect upon ovarian reserve such as some endocrinopathy, malign diseases which require radiotherapy and chemotherapy etc.

Study Design


Intervention

Procedure:
Hypogastric and/or uterine artery ligation


Locations

Country Name City State
Turkey Ege University, Medicine Faculty, Department of Obstetrics and Gynecology Izmir

Sponsors (1)

Lead Sponsor Collaborator
Ege University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anti-mullerian hormone levels will be evaluated 6 months after surgery and delivery
Primary Antral Follicule Count will be evaluated 6 months after surgery and delivery
Primary Ovarian volume will be evaluated 6 months after surgery and delivery
Primary Follicule Stimuli Hormone levels will be evaluated 6 months after surgery and delivery
Primary Estrogen levels will be evaluated 6 months after surgery and delivery
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