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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01982526
Other study ID # 2011-84
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2012
Est. completion date May 2016

Study information

Verified date August 2018
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

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.


Description:

long term results of the postoperative follow up for the endometrioma patients


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date May 2016
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 17 Years to 42 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Kanuni Sultan Suleyman Education and Research Hospital 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 Long term postoperative ovarian reserve outcomes of endometrioma patients by examining antimullerian hormone. 2 years
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