Using low dose injectable progesterone to trigger ovulation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of low dose injectable progesterone in triggering ovulation in women experiencing infertility. It focuses on women aged 20 to 35 with unexplained infertility and normal basal follicle-stimulating hormone levels. The study compares the outcomes of progesterone treatment against a placebo to determine its impact on ovulation induction. The research aims to provide insights into alternative methods for enhancing fertility in women undergoing assisted reproductive technologies.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Age from 20 to 35 years.
* Infertile women.
* Basal follicle-stimulating hormone (FSH) level \<10 mIU/ml.

Exclusion Criteria:

* Poor ovarian reserve.
* Immunological disease.
* Endometriosis.
* Uterine abnormality.
* Body mass index (BMI) \>30 kg/m2.
* Endometrial thickness \<8 or \>12 mm on the day of triggering.

Where it's running

• Teaching Hospitals and Institutes
  Cairo, Egypt Recruiting

Study contacts

• Study coordinator: Abeer A El Shabasi, MD
• Email: abear.elshabacy@gmail.com
• Phone: 00201223331182

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.