Overview
A randomized comparison of the live birth rate between the progestin-primed ovarian stimulation protocol and the gonadotrophin releasing hormone antagonist protocol in patients undergoing in vitro fertilization
Research question Does the live birth rate of the progestin-primed ovarian stimulation protocol comparable with the GnRH antagonist protocol for patients undergoing IVF?
Design This is a randomized controlled trial.
Research plan
Population: Infertile women who have medical indication for IVF will be recruited for study if they fulfil the selection criteria.
Intervention: Women will receive oral dydrogesterone 20mg daily from Day 3 till the day of ovulation trigger.
Comparator: Women will receive antagonist (Cetrorelix 0.25mg) once subcutaneously daily from day 6 of ovarian stimulation till the day of the ovulation trigger.
Outcomes: The primary outcome is the live birth rate the first FET.
Ovarian stimulation, egg retrieval, embryos frozen and frozen embryo transfer will be performed according to the standard operating procedures of the centres.
Eligibility
Inclusion Criteria:
- Age of women <43 years at the time of ovarian stimulation for IVF
- Antral follicle count (AFC) on day 2-5 of the period≥5
Exclusion Criteria:
- Presence of a functional ovarian cyst with E2>100 pg/mL
- Recipient of oocyte donation
- Undergoing preimplantation genetic testing
- Presence of hydrosalpinx which is not surgically treated or endometrial polyp on scanning during ovarian stimulation