drugset / Trial / NCT04797338

Gonadotropin Releasing Hormone Agonist (GnRHa) Versus Estrogen and Progesterone for Luteal Support in High Responders

NCT04797338

Phase 4 Unknown 100 enrolled Assaf-Harofeh Medical Center
RandomizedParallel-groupOpen-labelTreatment

Summary

Gonadotropin Releasing Hormone agonist (GnRHa) triggering is used as an alternative to human chorionic gonadotropin (hCG) in GnRH antagonist protocol to eliminate the risk of ovarian hyperstimulation syndrome (OHSS). However, its main disadvantage is a significantly lower pregnancy rate, hypothesized to result from a process called "luteolysis" (demise of the corpora lutea). In order to preserve a high pregnancy rates, several luteal support regimens were investigated, including an intensive estrogen and progesterone supplementation and a daily GnRHa treatment. However, no study, so far, compared the efficacy of these two regimens. Our aim is to compare the efficacy of GnRHa versus estrogen and progesterone supplementation for luteal phase support in high responders following GnRHa triggering.

Timeline

Start
2017-12-29
Primary completion
2021-09-30
Completion
2021-09-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator 17-alpha-hydroxyprogesterone caproate Unknown 250 mg Intramuscular
Comparator Estradiol Other / unclassified 4 mg Oral
Comparator Nafarelin Other / unclassified 200 ug Intranasal
Comparator Progesterone Other / unclassified 100 mg Other
Comparator Progesterone Other / unclassified 200 mg Other