Overview
Evaluation of the Optimal Dose of GnRH Agonist for Triggering Final Oocyte Maturation in High Risk OHSS Patients
Status:
Unknown status
Unknown status
Trial end date:
2016-07-01
2016-07-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The present study aims to investigate whether the dosage of the GnRH agonist used for triggering final oocyte maturation affects the maturity of the oocytes retrieved in high risk for OHSS patients undergoing ovarian stimulation for IVF using GnRH antagonists and recombinant FSH.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Aristotle University Of ThessalonikiCollaborator:
Eugonia IVF Unit, Athens, GreeceTreatments:
Deslorelin
Triptorelin Pamoate
Criteria
Inclusion Criteria: Patients undergoing ovarian stimulation for IVF using GnRH antagonistprotocol
- Age < 40 years
- Anticipated high ovarian response
Exclusion Criteria:
- Endometriosis > than grade II
- One ovary