← Back to Clinical Trials
Recruiting Phase 2, Phase 3 NCT07323329

Growth Hormone and Dehydroepiandrosterone Role in Vitro Fertilization

Trial Parameters

Condition Infertility
Sponsor Beni-Suef University
Study Type INTERVENTIONAL
Phase Phase 2, Phase 3
Enrollment 165
Sex FEMALE
Min Age 18 Years
Max Age 35 Years
Start Date 2025-10-10
Completion 2026-10-15
Interventions
Somatropin (4IU for 1 month) plus, folic acid 400 mcg per day.DHEA plus folic acid 400mcg per daycontrol group

Brief Summary

The goal of this study is to evaluate the role of Somatropin and Dehydroepiandrosterone (DHEA) on ovarian reserve parameters and intracytoplasmic sperm injection (ICSI) outcome in poor ovarian responder. The main question it aims to answer is: Which intervention is more effective in increasing number and size of follicles? Participants will be followed 1 month before starting induction in growth hormone and 12 weeks for DHEA and through intracytoplasmic sperm injection (ICSI) cycle.

Eligibility Criteria

Inclusion Criteria: At least two of the following three criteria had to be present after maximal stimulation: 1. Advanced maternal age (\>40 years) or any other risk factor for Poor Ovarian Response (POR). 2. ≤3 oocytes with a conventional stimulation protocol). 3. An abnormal ovarian reserve test \[i.e. antral follicle count (AFC) less than 5-7 follicles or anti-Müllerian hormone (AMH) below 0.5-1.1 ng/ml\]. Exclusion Criteria: 1. Any endocrine or metabolic disorder such as hyperprolactinemia, diabetes and thyroid dysfunction. 2. Any pelvic pathology such as hydrosalpinx, uterine anomaly. 3. Any male factor infertility such as Oligo-Astheno-Teratozoospermia (OAT) or azoospermia

Related Trials