IVF/ICSI infertility
Conditions
Interventions
Two different GnRH antagonist treatment protocols used in daily practice will
be compared. Patients will be randomized to receive one of the following two
treatments:
Early fixed start: start GnRH a
Sponsors
Universitair Medisch Centrum Utrecht
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Women
Exclusion criteria
Exclusion criteria: More than 2 previous unsuccessful IVF/ICSI cycles
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is the live birth rate per started cycle. Live birth from cryopreserved embryos originating from, and occurring within 6 months of the initial treatment cycle will be included in the total live birth rate per started cycle. | — |
Secondary
| Measure | Time frame |
|---|---|
| Ongoing, clinical and biochemical pregnancy rate Incidence of premature LH rise as detected on day of hCG administration LH, E2, P4 levels on CD2, CD6 and day of hCG administration Number of retrieved oocytes Total number of embryos available for transfer Number of embryos suitable for transfer Implantation rate per ET Endometrial thickness on ultrasound examination on day of oocyte pick-up QALY assessment | — |
Countries
Netherlands
Outcome results
None listed