Clinical Trials Directory

Trials / Completed

CompletedNCT01500863

Endometrial Receptivity After GnRH Agonist Triggering

Endometrial Receptivity After GnRH Agonist Triggering From Final Oocyte Maturation

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
35 (actual)
Sponsor
IVI Madrid · Academic / Other
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Accepted

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).

Conditions

Interventions

TypeNameDescription
DRUGhCGsingle shot of 6500 IU hCG s.c. at the time of triggering
DRUGtriptorelinsingle shot of 0.2mg triptorelin s.c. at the time of triggering
DRUGTriptorelin, estradiol valerate, micronized vaginal progesterone4mg of estradiol valerate per os plus 400mg micronized vaginal progesterone daily starting the day after OPU
DRUGtriptorelin, hCGsingle shot of 1500 IU hCG s.c. the day of OPU plus 4mg of estradiol valerate per os plus 400mg micronized vaginal progesterone daily starting the day after OPU
DRUGtriptorelin, hCGMultiple doses of 500 IU hCG (OPU, +4 and +7) and 4mg of estradiol valerate per os plus 400mg micronized vaginal progesterone daily starting the day after OPU
DRUGtriptorelin, recombinant LH300 IU recombinant LH every 48h and 4mg of estradiol valerate per os plus 400mg micronized vaginal progesterone daily starting the day after OPU

Timeline

Start date
2011-11-01
Primary completion
2012-05-01
First posted
2011-12-29
Last updated
2016-10-26

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT01500863. Inclusion in this directory is not an endorsement.