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NCT01941017 Clinical Trial

Evaluation of the Ovarian Reserve in Infertile Patients With Endometriosis

Endometriosis Clinical Trial

Official title:
Evaluation of the Ovarian Reserve in Infertile Patients With Endometriosis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01941017
Other study ID # EORIE
Secondary ID
Status Completed
Phase N/A
First received March 27, 2013
Last updated September 9, 2013
Start date April 2009
Est. completion date March 2012

Study information
Verified date September 2013
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority Egypt: Institutional Review Board
Study type Observational

Clinical Trial Summary

Comparison between Ovarian reserve markers in patients with minimal/mild endometriosis and patients with tubal factor infertility

Description:

Comparison between Ovarian reserve markers (laboratory or us) in patients with minimal/mild endometriosis and patients with tubal factor infertility including:

Cycle Day 2 or 3 FSH and E2, Serum AMH and antral follicular count

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date March 2012
Est. primary completion date November 2011
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria:

Age 18-35 years of age. Written and signed informed consent by the patient to participate in the study. Patients with regular menses, both ovaries, serum TSH within normal range, body mass index (BMI) <30 kg/m2 with normal sperm analysis of the husband.

Exclusion Criteria:

Patients with previous endocrine disorders. Cases in which the cause for infertility was other than endometriosis (except for patients with tubal obstruction, in the control group).

Patient with previous surgery for endometriosis.

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams University

Outcome
Type Measure Description Time frame Safety issue
Primary Assessment of ovarian reserve in the 2 groups Serum AMH and antral follicular count (AFC) 2 years No
Secondary Other Hormonal parameters Cycle day 2 or 3 FSH and E2 2 years No
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