Trigger Timing in Ovarian Stimulations

Recruiting N/A Interventional Study
IVF Outcome
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 42
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
834 (estimated)
Sponsor
Peking University Third Hospital · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age: ≥18 and \<42 years old * AFC: ≥5 and \<20 * AMH: ≥1.1 ng/mL and \<2.5 ng/mL * BMI: ≥18.5 Kg/m2 and \<29 Kg/m * First or second ART cycle * Regular menstrual cycles (between 22 and 35 days) * Two ovaries present * Planned for single or double day 3 transfer * Infertile cou…
Contacts

Rong Li, M.D.

+86-010-82265080

roseli001@sina.com

CONTACT

Lin Zeng, PhD

13810002416

zlwhy@163.com

CONTACT