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NCT03326024 Clinical Trial

The Ovarian Reserve and Laparoscopic Ovarian Drilling

Polycystic Ovary Syndrome Clinical Trial

Official title:
Long Term Assessment of Ovarian Reserve After More Than Two Years of Laparoscopic Ovarian Drilling in Polycystic Ovary Syndrome

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT03326024
Other study ID # 17100367
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 20, 2017
Last updated October 27, 2017
Start date November 1, 2017
Est. completion date October 1, 2018

Study information
Verified date October 2017
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Long term assessment of ovarian reserve after more than two years of laparoscopic ovarian drilling in Polycystic Ovary Syndrome

Description:

Inclusion criteria:

Goup "A": Patients with polycystic ovary syndrome at reproductive age (20-35) diagnosed according to Rotterdam criteria and underwent laparoscopic ovarian drilling from more than two years.

Goup "B": Patients with polycystic ovary syndrome at reproductive age (20-35) diagnosed according to Rotterdam criteria and didn't undergo laparoscopic ovarian drilling

Anti-mullerian hormone (as an indicator for ovarian reserve) will be measured for the two groups and data collected will be compared

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 90
Est. completion date October 1, 2018
Est. primary completion date October 1, 2018
Accepts healthy volunteers
Gender Female
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- Goup "A": Patients with polycystic ovary syndrome at reproductive age (20-35) diagnosed according to Rotterdam criteria and underwent laparoscopic ovarian drilling from more than two years.

Goup "B": Patients with polycystic ovary syndrome at reproductive age (20-35) diagnosed according to Rotterdam criteria and didn't undergo laparoscopic ovarian drilling

Exclusion Criteria:

1. Age <19 or > 35 years.

2. BMI <19 or > 35

3. patients refusing to participate in the study.

4. previous ovarian cystectomy.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Outcome
Type Measure Description Time frame Safety issue
Primary Level of anti-mullerian hormone after laparoscopic ovarian drilling 2 years
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