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NCT03907605 Clinical Trial

Anti-Mullerian Hormone (AMH) is a Marker for Ovarian Reserve. There Are Many Studies About AMH Changes in Ovarian Surgery, But Little is Known for Other Surgeries. We Seek to Investigate the Hormone Variations Before and After Uterine Artey Ligation for Postpartum Hemorrage (PPH)

Post Partum Hemorrhage Clinical Trial

Official title:
Comparison of Serum Anti-Mullerian Hormone Levels Following Uterine Artery Ligation for PPH.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03907605
Other study ID # amhpph
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2018
Est. completion date April 1, 2019

Study information
Verified date April 2019
Source Kanuni Sultan Suleyman Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Anti-Mullerian hormone (AMH) is a marker for ovarian reserve. There are many studies about AMH changes in ovarian surgery, but little is known for other surgeries. We seek to investigate the hormone variations before and after uterine artey ligation for postpartum hemorrage (PPH)

Description:

All patients belong to the same group. The blood samples will be collected at the time of surgery and 3 months after surgery from the patients who need uterine artery ligation for PPH. The blood samples will be centrifuged within 2 hours after being obtained and assessed on the same day. AMH concentrations will be measured with an enzymatically amplified two-sided immunoassay

Recruitment information / eligibility
Status Completed
Enrollment 88
Est. completion date April 1, 2019
Est. primary completion date March 1, 2019
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 uterine artery ligation due to PPH

Exclusion Criteria:

- Pregnancy with IVF or oosit donation

- Patients with endocrinopathy, diseases which require radiotherapy and chemotherapy etc.

- Patients with BMI >40

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• anti- mullerian hormone
All patients belong to the same group. The blood samples will be collected at the time of surgery and 3 months after surgery from the patients who need uterine artery ligation for PPH. The blood samples will be centrifuged within 2 hours after being obtained and assessed on the same day. AMH concentrations will be measured with an enzymatically amplified two-sided immunoassay

Locations
Country Name City State
Turkey Pinar Yalcin Bahat Istanbul I?stanbul

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 1- Anti-Mullerian Hormone levels variation Anti-Mullerian Hormone levels before and 3 months after surgery 3 months
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