Overview

Comparing the Efficacy of Urinary and Recombinant Human Chorionic Gonadotropin (hCG) on Oocyte Maturity

Status:
Completed
Trial end date:
2013-06-01
Target enrollment:
0
Participant gender:
Female
Summary
This study is a prospective randomized clinical trial to compare the efficacy of the urinary and recombinant hCG on oocyte quality for ovulation induction in women undergoing IVF/ICSI.
Phase:
Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Royan Institute
Treatments:
Chorionic Gonadotropin
Criteria
Inclusion Criteria:

- Indication for IVF/ICSI and Long Protocol ovarian stimulation

- Age 20-37

- Body mass index (BMI) ≤ 30 kg/m2

- Regular menstrual cycles of 25-35 days

- Tubal or male factor

- Existence of both ovary and normal uterine cavity

- Basal FSH≥10

- Physical health

Exclusion Criteria:

- Poly Cystic Ovarian Syndrome patients

- Contraindications of gonadotropins administration

- Poor response to ovulation induction in recent cycle