- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01982526
Role of Anti Mullerian Hormone for Ovarian Reserve Determination of Preoperative and Postoperative Endometrioma Patients
August 8, 2018 updated by: Ergul Demircivi Bor, Kanuni Sultan Suleyman Training and Research Hospital
Ovarian reserve influenced by many factor but especially cysts like endometrioma.
Anti mullerian hormone is recent marker for ovarian reserve.
The investigators are searching ovarian reserve pre and post operatively by using antimullerian hormone of endometrioma patient who are operated for their cysts.
Study Overview
Status
Completed
Conditions
Detailed Description
long term results of the postoperative follow up for the endometrioma patients
Study Type
Observational
Enrollment (Actual)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Istanbul, Turkey, 34303
- Kanuni Sultan Suleyman Education and Research Hospital
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
17 years to 42 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Females who are administring gynecology clinic suffering from symptomatic benign ovarian cysts.
Description
Inclusion Criteria:
- Ultrasonographical symptomatic and benign cysts which has surgery indication.
Exclusion Criteria:
- Over 42 years old, systemic endocrine disorder, history of ovarian surgery
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Endmetrioma surgery
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Long term postoperative ovarian reserve outcomes of endometrioma patients by examining antimullerian hormone.
Time Frame: 2 years
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2012
Primary Completion (Actual)
May 1, 2013
Study Completion (Actual)
May 1, 2016
Study Registration Dates
First Submitted
November 6, 2013
First Submitted That Met QC Criteria
November 12, 2013
First Posted (Estimate)
November 13, 2013
Study Record Updates
Last Update Posted (Actual)
August 10, 2018
Last Update Submitted That Met QC Criteria
August 8, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2011-84
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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