Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06023602
NA

Effectiveness of Generic Versus Reference Cetrorelix Acetate for Ovarian Stimulation Using a Gonadotropin-releasing Hormone(GnRH)Antagonist Protocol in Women Undergoing IVF

Sponsor: Northwest Women's and Children's Hospital, Xi'an, Shaanxi

View on ClinicalTrials.gov

Summary

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.

Official title: Effectiveness of Generic Cetrorelix Acetate Versus Reference Cetrorelix Acetate for Ovarian Stimulation Using a GnRH Antagonist Protocol in Women Undergoing IVF: A Multicenter Non-inferiority, Randomised Controlled Trial

Key Details

Gender

FEMALE

Age Range

20 Years - 42 Years

Study Type

INTERVENTIONAL

Enrollment

1338

Start Date

2024-02-27

Completion Date

2025-12-01

Last Updated

2025-09-19

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

Generic cetrorelix acetate

Generic cetrorelix acetate (0.25 mg SC)

DRUG

Reference cetrorelix acetate

reference cetrorelix acetate (0.25 mg SC)

Locations (1)

He Cai

Xi'an, None Selected, China