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Triptorelin

Decapeptyl, Trelstar, Gonapeptyl, Pamorelin

Quick Stats
Studies 178
Trials 100
Completed NA INTERVENTIONAL NCT00516490

GnRH Agonist Administration in the Luteal Phase of ICSI-ET Cycles

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

A single dose GnRH agonist administration in the luteal phase of assisted reproduction cycles was reported to increase pregnancy and birth rates. This study was done to evaluate the reproducibility of previous findings.

Detailed Description

GnRH agonist administration in the luteal phase was reported to beneficially affect clinical outcome of ICSI-ET cycles. This randomized controlled trial evaluates the effect of a single dose GnRH agonist administered in the luteal phase on the outcome of ICSI - ET cycles stimulated with the long GnRH agonist protocol. Women undergoing embryo transfer following controlled ovarian hyperstimulation with a long GnRH agonist protocol were included. In addition to routine luteal phase support with progesterone women were randomized to receive a single dose of GnRH agonist or placebo on the sixth day after ICSI.Ongoing pregnancy rate was the primary outcome measure.

Interventions

Name: triptorelin acetate
Type: DRUG
Description: Single dose of 0.1 mg triptorelin subcutaneous injection on the 3rd day after embryo transfer
Name: Na Cl %0.9
Type: DRUG
Description: 0.1 ml sterile saline subcutaneous injection on the 3rd day after embryo transfer

Primary Outcomes

Measure: Ongoing pregnancy rate beyond 20 weeks
TimeFrame:
Description:

Trial Information

NCT ID

NCT00516490

Status

Completed

Study Type

INTERVENTIONAL

Phases

NA

Sponsor

V.K.V. American Hospital, Istanbul

Last Updated

December 15, 2025