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IVF Outcomes With Time-Lapse Culture: Comparison Between PPOS and GnRH Antagonist Protocols

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

Design: Researchers will randomly assign 148 women undergoing IVF to two groups: * PPOS group (n=74): Will receive FSH injections (oral Duphaston 20mg daily) starting from day 2-3 of the menstrual cycle * GnRH Antagonist group (n=74): Will receive FSH injections (Orgalutran 0.25mg injections) when follicles reach ≥14mm Participants will: * Undergo controlled ovarian stimulation with their assigned protocol for approximately 10-12 days * Have regular ultrasound monitoring and blood tests to track follicle development * Undergo egg retrieval procedure when follicles are mature * Have all embryos cultured in the EmbryoScope time-lapse incubator with continuous monitoring * Have embryos frozen on Day 5/6 for future transfer Study Location: Department of Assisted Reproduction and Andrology, Hanoi Obstetrics and Gynecology Hospital Study Duration: January 2026 - June 2028

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 20
Maximum Age: 45
Healthy Volunteers: f
View:

• Women aged 20-45 years

• Indicated for in vitro fertilization (IVF) treatment

• Planned freeze-all embryo strategy

• Voluntary participation in research.

Locations
Other Locations
Viet Nam
Hanoi Obstetrics and Gynecology Hospital
RECRUITING
Hanoi
Contact Information
Primary
Thanh Huy Dao, MD
huythanhdao.hmu@gmail.com
+84 971597096
Time Frame
Start Date: 2026-01-21
Estimated Completion Date: 2028-10
Participants
Target number of participants: 148
Treatments
Experimental: PPOS protocol
FSH + Dydrogesterone 20mg/day from day 2 - 3 of the menstrual cycle. Optional LH supplementation. Freeze-all with time-lapse monitoring.
Active_comparator: Antagonist protocol
FSH + Orgalutran 0.25 mg/day (starting when follicle ≥12 mm). Optional LH supplementation. Freeze-all with time-lapse monitoring.
Related Therapeutic Areas
Sponsors
Leads: Hanoi Medical University
Collaborators: Hanoi Obstetrics and Gynecology Hospital

This content was sourced from clinicaltrials.gov