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A Comparative Study of In Vitro Fertilization Outcomes Between PPOS and Antagonist Protocols in Women With Polycystic Ovary Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 40
Healthy Volunteers: f
View:

• 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 alone or PCOS with other infertility factors (e.g., tubal factor, previous failed IUI)

• Eligible for controlled ovarian stimulation for IVF

• Husband/partner with normal sperm parameters or mild to moderate oligoasthenoteratozoospermia (OAT)

• Willing and able to provide written informed consent and comply with study procedures.

Locations
Other Locations
Viet Nam
Hanoi General Hospital
RECRUITING
Hanoi
Contact Information
Primary
Phuong Duy Nguyen, MD, MS
nguyenduyphuongncs44@gmail.com
+84 986656835
Time Frame
Start Date: 2026-01-20
Estimated Completion Date: 2028-06-30
Participants
Target number of participants: 400
Treatments
Experimental: PPOS Protocol
Participants receive ovarian stimulation using the progestin-primed ovarian stimulation (PPOS) protocol for in vitro fertilization.
Active_comparator: GnRH Antagonist Protocol
Participants receive ovarian stimulation using a GnRH antagonist protocol for in vitro fertilization.
Sponsors
Leads: Hanoi General Hospital (Vietnam)

This content was sourced from clinicaltrials.gov