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The effect of GnRH analog on the results of frozen-thawed embryo transfers.

GnRH analog as a luteal phase support in frozen-thawed embryo transfer cycles. A Pilot study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2013-000106-29-FI
Enrollment
240
Registered
2013-02-20
Start date
2013-03-19
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Infertility MedDRA version: 14.1 Level: LLT Classification code 10042391 Term: Subfertility System Organ Class: 100000004872

Interventions

Trade Name: Gonapeptyl 0.1 mg/mi inj Pharmaceutical Form: Injection INN or Proposed INN: TRIPTORELIN ACETATE CAS Number: 140194-24-7

Sponsors

Turku University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 20 - 45 year old women coming to frozen thawed embryo transfer. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 240 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: The age of the woman over 42 year during the initial IVF/ICSI-treatment, from which the embryos derive. Abnormal uterus Known abnormality of karyotype of the woman or her partner Severe male factor as an exclusive reason for subfertillity Allergy for Gonapeptyl

Design outcomes

Primary

MeasureTime frame
Main Objective: To compare the results of frozen.thawed embryo transfers with and without GnRH analog support;Secondary Objective: S-hCG, S-Prog S-E2 The lenght of the luteal phase Bleeding in luteal phase;Primary end point(s): Pregnancy rate, implantation rate, miscarriages, live birth rate, multiple birth rate;Timepoint(s) of evaluation of this end point: One year after the last embryo transfer

Secondary

MeasureTime frame
Secondary end point(s): S-hCG, S-Prog S-E2 The lenght of the luteal phase Bleeding in luteal phase;Timepoint(s) of evaluation of this end point: Within a year from the last embryo transfer

Countries

Finland

Contacts

Public ContactVarpu Jokimaa

Turku University Hospital

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026