RecruitingPhase 3NCT04064840

GnRH Agonist for Dual Trigger in IVF and for Luteal Phase Support in FET

Gonadotrophin Releasing Hormone Agonist for Dual Trigger in in Vitro Fertilization and for Luteal Phase Support in Frozen-thawed Embryo Transfer


Sponsor

The University of Hong Kong

Enrollment

784 participants

Start Date

Sep 1, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

The objectives of this study are to compare the efficacy of the dual trigger group vs the hCG trigger group on the live birth rate in women undergoing IVF and the efficacy of the agonist in LP group vs the placebo group on the live birth rate in women undergoing FET.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 42 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called FET: Decapeptyl, a drug called FET: Normal Saline, and others for people with subfertility. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 42 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGIVF: Decapeptyl and hCG

When at least three follicles reach 18 mm in diameter, recombinant hCG 0.25mg and decapeptyl 0.2mg will be injected subcutaneously.

DRUGFET: Decapeptyl

On the day of FET, decapeptyl 0.1 mg will be injected subcutaneously.

DRUGIVF: hCG and normal saline

When at least three follicles reach 18 mm in diameter, recombinant hCG 0.25mg and normal saline will be injected subcutaneously.

DRUGFET: Normal Saline

On the day of FET, normal saline will be injected subcutaneously.


Locations(1)

Department of Obstetrics and Gynaecology

Hong Kong, Hong Kong, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04064840


Related Trials