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Triptorelin

Decapeptyl, Trelstar, Gonapeptyl, Pamorelin

Quick Stats
Studies 178
Trials 100
Score 1
2022 pubmed

GnRH agonist administration as luteal support on the transfer day of single blastocyst in dual-triggered cycles.

Demir. Ahmet A; Köse. Can C; Şahin Güleç. Ebru E; Türkmen. Pınar P; Töz. Emrah E; Peker. Nuri N

Key Findings

  • Adding a single 0.1 mg dose of triptorelin to routine progesterone luteal support did not raise beta‑hCG positivity rates.
  • Clinical pregnancy rates were essentially unchanged between the triptorelin group and the control group.
  • Live‑birth rates were also similar, with no statistical benefit from the extra peptide.

Practical Outcomes

  • For people experimenting with health protocols, this study suggests that using triptorelin as an extra luteal‑phase supplement in IVF does not improve outcomes and is not a worthwhile addition. Stick with the standard progesterone regimen unless new evidence emerges.

Summary

A study looked at whether giving a single shot of the peptide drug triptorelin (a GnRH agonist) on the day a frozen embryo is transferred would boost pregnancy success in IVF cycles. The researchers found no meaningful improvement in pregnancy tests, clinical pregnancy, or live‑birth rates compared to standard progesterone support alone.

Abstract

Luteal phase support with gonadotropin-releasing hormone agonist (GnRH-a) has been considered in terms of its potential beneficial effects on in vitro fertilisation (IVF) cycles. In our study, we assessed the effectiveness of single-dose GnRH-a administration in dual-triggered cycles on pregnancy outcomes. Eighty women who underwent intra cytoplasmic sperm injection (ICSI) cycle and had fresh blastocyst transfer were divided into two groups in terms of luteal phase support. The study group (Group A) consisted of patients (n = 40) who received a single-dose GnRH-a injection (0.1 mg of triptorelin acetate) subcutaneously 6 days after oocyte retrieval in addition to 600 mg daily of micronised progesterone, and the control group (Group B) comprised of patients (n = 40) taking 600 mg micronised progesterone daily from the first day after oocyte retrieval. GnRH-a and human chorionic gonadotropin (hCG; dual trigger) were administered to all patients. Comparison of the clinical pregnancy and live birth rates was our main goal. There was no significant difference between the two groups in terms of β-hCG positivity rates, clinical pregnancy rates and live birth rates (p value for beta-hCG = 0.25, clinical pregnancy = 0.80, live birth = 0.45). Our study demonstrated that in dual triggered cycles administration of a single dose of GnRH-a on the transfer day of a single blastocyst in addition to routine luteal phase support with progesterone does not statistically increase implantation, clinical pregnancy or live birth rates.

Study Information

Provider

pubmed

Year

2022

Date

2022-08-23T00:00:00.000Z

DOI

10.5603/gp.a2022.0082