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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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02995343
Study type Interventional
Source Ege University
Contact cagdas sahin, MD
Phone +905324676106
Email [email protected]
Status Recruiting
Phase N/A
Start date November 2016
Completion date September 2019

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