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)
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| ClinicalTrials.gov Identifier: NCT03907605 |
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Recruitment Status :
Completed
First Posted : April 9, 2019
Last Update Posted : April 9, 2019
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| Condition or disease | Intervention/treatment |
|---|---|
| Anti-Mullerian Hormone Deficiency Post Partum Hemorrhage | Other: anti- mullerian hormone |
| Study Type : | Observational |
| Actual Enrollment : | 88 participants |
| Observational Model: | Cohort |
| Time Perspective: | Retrospective |
| Official Title: | Comparison of Serum Anti-Mullerian Hormone Levels Following Uterine Artery Ligation for PPH. |
| Actual Study Start Date : | March 1, 2018 |
| Actual Primary Completion Date : | March 1, 2019 |
| Actual Study Completion Date : | April 1, 2019 |
- 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
- 1- Anti-Mullerian Hormone levels variation [ Time Frame: 3 months ]Anti-Mullerian Hormone levels before and 3 months after surgery
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| Ages Eligible for Study: | 18 Years to 40 Years (Adult) |
| Sexes Eligible for Study: | Female |
| Gender Based Eligibility: | Yes |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
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
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03907605
| Turkey | |
| Pinar Yalcin Bahat | |
| Istanbul, İ̇stanbul, Turkey, 34000 | |
| Responsible Party: | Pınar Yalcin bahat, Principal Investigator, Kanuni Sultan Suleyman Training and Research Hospital |
| ClinicalTrials.gov Identifier: | NCT03907605 |
| Other Study ID Numbers: |
amhpph |
| First Posted: | April 9, 2019 Key Record Dates |
| Last Update Posted: | April 9, 2019 |
| Last Verified: | April 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Yes |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Postpartum Hemorrhage Hemorrhage Pathologic Processes Obstetric Labor Complications Pregnancy Complications |
Puerperal Disorders Uterine Hemorrhage Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs |

