drugset / Trial / NCT01500863

Endometrial Receptivity After GnRH Agonist Triggering

NCT01500863

Phase 4 Completed 35 enrolled IVI Madrid
RandomizedFactorialSingle-blindTreatment

Summary

Conventional luteal phase support after human chorionic gonadotrophin (hCG) triggering in women undergoing in vitro fertilization/intracytoplasmic sperm injection (IVF/ICSI) provides adequate pregnancy rates and live birth rates, but Ovarian hyperstimulation syndrome (OHSS) still occurs in 1-3% of the patients. If gonadotropin-releasing hormone agonist (GnRHa) are used instead of hCG, OHSS does not occur, but clinical results are somehow diminished. By testing different luteal support protocols on women undergoing GnRHa triggering, the investigators aim to find out which protocol resembles the most the gene expression profile observed after hCG triggering and conventional luteal phase support, in order to choose it as the most adequate in terms of endometrium receptivity and safety (OHSS incidence).

Timeline

Start
2011-11
Primary completion
2012-05
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Progesterone Other / unclassified 400 mg Other
Subject Recombinant LH Protein / enzyme biologic 300 iu
Subject Triptorelin Other / unclassified 0.2 mg Subcutaneous
Subject estradiol valerate Unknown 4 mg Oral
Comparator hCG Unknown 500 iu Subcutaneous
Comparator hCG Unknown 1500 iu Subcutaneous
Comparator hCG Unknown 6500 iu Subcutaneous