Effectiveness of Generic Versus Reference Cetrorelix Acetate for Ovarian Stimulation Using a Gonadotropin-releasing Hormone（GnRH）Antagonist Protocol in Women Undergoing IVF
Recruiting now · Not applicable
Conditions studied: Infertility
In brief
The goal of this clinical trial is to compare the clinical outcomes using different cetrorelix acetate in the context of a GnRH antagonist protocol for ovarian stimulation in women undergoing IVF or intracytoplasmic sperm injection(ICSI) treatment.The main question it aims to answer is whether the generic cetrorelix acetate is non-inferior to the reference product in the GnRH antagonist based protocol for women undergoing IVF. Ovarian stimulation was achieved by several types of follicle-stimulating hormone(FSH) or by FSH combined with luteinizing hormone activity. Daily dose of generic cetrorelix acetate (0.25 mg SC) or original cetrorelix acetate (0.25 mg SC) will be administered when the lead follicle was 14 mm. When more than two follicles reached 17 mm, oocyte maturation was triggered with 250 mcg of recombinant human chorionic gonadotropin.
Key facts
- Study ID
- NCT06023602
- Run by
- Northwest Women's and Children's Hospital, Xi'an, Shaanxi
- People needed
- 1338
- Starts
- 2024-02-27
- Expected to finish
- 2025-12-01
- Last updated by the study team
- 2025-09-19
Who can join
Age: 20 and older, up to 42. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Infertile couples plan to undergo IVF / ICSI pregnancy treatment into screening procedures and clinical study
- All subjects should sign the informed consent form
- Infertile women <43 years old
- With flexible GnRH antagonist
You may not qualify if…
- Subjects could not enter the study if they meet any one of the following criteria
- Preimplantation Genetic Testing (PGT)
- Untreated hydrosalpinges, moderate or severe endometriosis, recurrent spontaneous miscarriage, endometrial pathology, uterine malformations, etc
- Endocrine diseases (such as hyperthyroidism, hyperprolactinemia, etc.) or other systemic disease and other systemic diseases (such as hypertension, diabetes, etc.)．
- Other factors were considered inappropriate by the investigator to participate, or assisted reproductive technology/pregnancy contraindications
Where it is running
- He Cai — Xi'an, None Selected, China (enrolling)
Full record on ClinicalTrials.gov
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