Overview
GNRH Agonist Trigger and Modified Luteal Phase Adding a Bolus of GnRHa at the Time of Implantation: a RCT
Status:
Completed
Completed
Trial end date:
2017-03-01
2017-03-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
Purpose:The aim of this project is to prospectively determine whether a single dose of GnRH-agonist administered at the time of implantation increases or not the reproductive outcome in patients undergoing in vitro fertilization ( IVF)/ intracytoplasmatic sperm injection(ICSI) triggered by a GnRH-agonist followed by a small bolus of human chorionic gonadotropin (hCG 1500 IU) the day of oocyte retrieval.Phase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Centre Hospitalier Universitaire Ibn RochdTreatments:
Deslorelin
Triptorelin Pamoate
Criteria
Inclusion Criteria:Female age < 40 years No uterine (fibroids, mullerian malformations), ovarian (
endometrioma) or adnexa (hydrosalpinx) abnormalities• Baseline FSH and LH < 12
IU/l.Patients with at least one embryo at transfer time
Exclusion Criteria:
- Very high risk of OHSS (> 30 follicles > 12 mm the day of ovulation triggering). •
Reduced ovarian reserve
- Fertilization failure
- Severe endocrinopathy
- Azoospermia