Comparison of IVF Outcomes Between PPOS and Antagonist Protocols in Women With PCOS
Recruiting
N/A
Interventional Study
Polycystic Ovary Syndrome (PCOS)
Female Infertility
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 40
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 400 (estimated)
- Sponsor
- Hanoi General Hospital (Vietnam) · Other
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About This Trial
This study aims to compare the outcomes of two ovarian stimulation protocols used in in vitro fertilization (IVF): the progestin-primed ovarian stimulation (PPOS) protocol and the GnRH antagonist protocol.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Women aged 18-40 years
* Diagnosed with polycystic ovary syndrome (PCOS) according to the modified Rotterdam criteria (2004) (≥2 of 3: oligo/anovulation, hyperandrogenism, or polycystic ovarian morphology on ultrasound)
* Indicated for in vitro fertilization (IVF) due to PCOS …
Contacts