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Completed

NCT Number: NCT01941017

Evaluation of the Ovarian Reserve in Infertile Patients With Endometriosis

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

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Key information

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Assessment of ovarian reserve in the 2 groups

    Time frame: 2 years

    Serum AMH and antral follicular count (AFC)

Secondary outcomes

  1. Other Hormonal parameters

    Time frame: 2 years

    Cycle day 2 or 3 FSH and E2

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Important dates

Study start
2009
Primary completion
2011
Study completion
2012
First posted
Sep 13, 2013
Registry last updated
Sep 13, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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