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Triptorelin

Decapeptyl, Trelstar, Gonapeptyl, Pamorelin

Quick Stats
Studies 178
Trials 100
Completed PHASE4 INTERVENTIONAL NCT00461916

Half-Dose Depot Triptorelin Versus Reduced-Dose Daily Buserelin

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

The purpose of this study is to determine whether half-dose depot triptorelin are as effective as reduced-dose daily buserelin in the controlled ovarian stimulation for intracytoplasmic sperm injection and embryo transfer

Detailed Description

Significant doubts remain about which type of GnRH agonists \[GnRHa\] administration to be used in controlled ovarian stimulation \[COS\] cycles. The use of a single-dose depot long-acting GnRHa instead of a daily low dose preparation would be more comfortable for patients, however, inducing a profound pituitary desensitization, it increases the number of gonadotropin ampoules and the duration of the COS cycle without improving pregnancy rates or other clinical outcomes. Thus, some authors recommend a reduction of both dose and/or duration of GnRHa administration. Halving the dose of depot triptorelin, for instance, has been studied against its full dose administration since 1992 with rather similar clinical outcomes. Half-dose depot leuprolide acetate has also resulted in comparable clinical outcomes with standard daily injections in long GnRHa protocol. Reducing the daily doses of short acting GnRHa has been advocated to demonstrate equivalent results to standard doses. To our knowledge, however, the reduced daily doses have not been evaluated against half dose depot forms in long GnRHa protocols. Thus, we originally compared a half-dose depot triptorelin with reduced daily doses of short-acting buserelin in a long protocol for intracytoplasmic sperm injection and embryo transfer \[ICSI/ET\] cycles.

Interventions

Name: Half-Dose Depot Triptorelin
Type: DRUG
Description:
Name: Reduced-Dose Daily Buserelin
Type: DRUG
Description:

Primary Outcomes

Measure: Number of retrieved oocytes
TimeFrame:
Description:

Trial Information

NCT ID

NCT00461916

Status

Completed

Study Type

INTERVENTIONAL

Phases

PHASE4

Sponsor

Tehran University of Medical Sciences

Last Updated

December 15, 2025