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Prospective, multicenter, randomized controlled trial towards identifying the optimal Cetrotide treatment protocol

Prospective, multicenter, randomized controlled trial towards identifying the optimal Cetrotide treatment protocol - CETRO Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON37107
Enrollment
2430
Registered
2008-08-11
Start date
2009-03-12
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

IVF/ICSI infertility

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
Lead Sponsor

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

MeasureTime 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

MeasureTime 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

Source: NL-OMON (via WHO ICTRP)