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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03220594
Other study ID # 1826
Secondary ID
Status Completed
Phase N/A
First received July 14, 2017
Last updated September 29, 2017
Start date March 20, 2017
Est. completion date September 29, 2017

Study information

Verified date September 2017
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

To observe the effects of hypogastric artery ligation on serum antimullerian hormone levels.


Description:

To measure and compare serum antimullerian hormone levels in patients who underwent hypogastric artery ligation/ hypogastric artery ligation+ hysterectomy and postpartum control. The procedures performed as an emergency life saving method during delivery. The reasons for hypogastric artery ligation/ hypogastric artery ligation+ hysterectomy were obstetric hemorrhage mainly uterine atony.

The serum levels of antimullerian hormone were measured 6 months after the operations and compared with matching postpartum controls. Serum levels of FSH, LH, PRL and TSH were also measured 6 months after the operation. Further, antral follicle count measured along with the aforementioned blood tests.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date September 29, 2017
Est. primary completion date September 20, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- age 18- 40 years

- no systemic or endocrine diseases

- patients who had hypogastric artery ligation and/or hysterectomy

- healthy postpartum patients as controls

Exclusion Criteria:

- history of chemotherapy and/or radiotherapy

- Obese patients

- patients with previous/present endometriosis

- patients with PCOS

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
hypogastric artery ligation
hypogastric artery ligation is the ligation of the internal iliac artery to stop bleeding related to obstetrics obstetric hemorrhage Hysterectomy is the removal of the uterus if bleeding can't stop by hypogastric artery ligation

Locations

Country Name City State
Turkey Kanuni SSTRH Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Kanuni Sultan Suleyman Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ovarian reserve To evaluate postoperative ovarian reserve using anti-mullerian hormones and other ovary related hormones including FSH,LH 6 months
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