Actively Recruiting

Phase Not Applicable
Age: 20Years - 45Years
FEMALE
NCT07409493

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

Led by Hanoi Medical University · Updated on 2026-02-13

148

Participants Needed

1

Research Sites

140 weeks

Total Duration

On this page

Sponsors

H

Hanoi Medical University

Lead Sponsor

H

Hanoi Obstetrics and Gynecology Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare two ovarian stimulation protocols used in in vitro fertilization (IVF): the fixed Progestin-Primed Ovarian Stimulation (PPOS) protocol and the GnRH Antagonist protocol. The study will evaluate IVF outcomes and embryo development patterns using time-lapse embryo monitoring technology. The main questions the study aims to answer are: * Does the fixed - PPOS protocol achieve similar numbers of mature eggs, good-quality embryos, and clinical outcomes compared to the GnRH Antagonist protocol? * Are there differences in embryo development patterns (morphokinetics) between the two protocols when monitored by time-lapse imaging? * How does embryo quality (KIDScore) compare between the two protocols? Study 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

CONDITIONS

Official Title

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

Who Can Participate

Age: 20Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 20 to 45 years
  • Planned to undergo in vitro fertilization (IVF) treatment
  • Planned freeze-all embryo strategy
  • Voluntarily agree to participate in the research
Not Eligible

You will not qualify if you...

  • Presence of systemic diseases
  • Use of hormonal medications within 3 months prior to enrollment
  • Participation in oocyte donation cycles
  • Unwilling or unable to participate in the research

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Trial Site Locations

Total: 1 location

1

Hanoi Obstetrics and Gynecology Hospital

Hanoi, Vietnam, 100000

Actively Recruiting

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Research Team

T

Thanh Huy Dao, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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