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Evaluation of the Ovarian Reserve in Patients Who Hypogastric Arteries and or Uterine Arteries Had Been Ligated

E

Ege University

Status

Unknown

Conditions

Uterine Artery Ligation
Ovarian Reserve
Hypogastric Artery Ligation

Treatments

Procedure: Hypogastric and/or uterine artery ligation

Study type

Interventional

Funder types

Other

Identifiers

NCT02995343
2.100.2014.0076

Details and patient eligibility

About

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

Enrollment

40 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Hypogastric and/or uterine artery ligation
Experimental group
Description:
Patients who had been ligated hypogastric artery and or uterine artery for ceasing uterine bleeding during c-section
Treatment:
Procedure: Hypogastric and/or uterine artery ligation
Normal postpartum women
No Intervention group

Trial contacts and locations

1

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Central trial contact

cagdas sahin, MD

Data sourced from clinicaltrials.gov

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