← Eichor
Study identifier: NCT04163133 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Trigger Timing in Ovarian Stimulations

Condition: IVF Outcome  ·  Sponsor: Peking University Third Hospital

PhaseNA
Planned participants834
Who can joinFemale, 18 Years to 42 Years
Healthy volunteersNo

About this study

The use of antagonist ovulation stimulation program is increasing year by year, because of its convenience, flexibility, and prevention effect of ovarian hyperstimulation syndrome. However, many researchers and clinicians believe that the clinical outcomes of antagonist regimens are worse than those of classical long-term regimens. Studies showed that the reasons for that maybe antagonist protocol results in poor effect on oocytes maturation or endometrial receptivity. At present, the trigger time of antagonist regimen is more than three follicles with diameters of ≥17 mm, which makes the duration of gonadotrophin application in antagonist regimen is shorter than that of long regimen. Whether the trigger time of antagonist regimen is too early to cause adverse effects on oocytes, embryos and eventual clinical outcomes is unknown. This study hopes to compare regular trigger timing and 1~2 days delay of trigger in ovarian stimulations by antagonist protocol,in order to study whether delay 1~2 days of trigger will get better clinical outcomes than regular trigger timing in ovarian stimulations by antagonist protocol in in vitro fertilization (IVF)/Intracytoplasmic sperm injection (ICSI). The results of this study will help infertile couples and clinicians to know and choose the optimal treatment in antagonist protocol.

This description comes directly from the study's public registry record.

Talk to the study team

Rong Li, M.D.  ·  +86-010-82265080  ·  roseli001@sina.com

Lin Zeng, PhD  ·  13810002416  ·  zlwhy@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Peking Univesity Third HospitalBeijing, Beijing Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04163133