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Use of GM-CSF Treatment in Recurrent Implantation Failure

Administration of GM-CSF in Women With Recurrent Implantation Failure in IVF Cycles and Egg Donation Cycles

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01715974
Enrollment
140
Registered
2012-10-29
Start date
2017-12-12
Completion date
2022-08-31
Last updated
2022-07-20

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

Conditions

Women With Recurrent Implantation Failure in IVF

Keywords

GM-CSF, IVF failure,pregnancy

Brief summary

The purpose of this study is to determine whether in Assisted Reproductive Technologies the treatment with GM-CSF, a growth factor working on stem cells, may improve the pregnancy rate and pregnancy outcome in patients experiencing recurrent implantation failure in IVF cycles.

Detailed description

The GM-CSF is a cytokine promoting leukocyte growth, but also trophoblast development. In this randomized sudy investigators will test this cytokine as a treatment for recurrent implantation failure after IVF, at leat three failed previous IVF attempts. The study will be conducted in 100 women with recurrent implantation failure of egg donation cycles. The inclusion criteria will be, at least three previous failed Egg Donation attempts where at least 4 good blastocysts were transferred, women less than 50 years old, absence of systemic diseases. These women will undergo egg donation cycle and they will randomly divided in two groups: one (50 women) will be treated with subcutaneous GM-CSF 60 micrograms/day from the day of transfer to the day of β-hCG test, and if it will be positive the treatment will be continued for other 40 days; the group of control will be treated with subcutaneous saline solution infusion in the same way of the study group. Primary outcomes will be considered: pregnancy rate and live birth rate, the of β-hCG levels at 14/21/28 and 35 days after embryo transfer.

Interventions

30 micrograms/day of GM-CSF from the day of embryo transfer through the day of beta HCG test

DRUGCONTROL

saline infusion every day from the day of embryo transfer through the day of beta HCG test

Sponsors

Centre for Endocrinology and Reproductive Medicine, Italy
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* women 50 years old or less with three or more previous egg donation cycles failed, * with a total of at least 4 blastocysts replaced in uterus

Exclusion criteria

* chromosomal defects in the patients, * metabolic diseases (diabetes etc.) * genetic diseases (thalassemia, cystic fibrosis, etc.)

Design outcomes

Primary

MeasureTime frameDescription
pregnancy outcome12 monthsThe number of patients pregnant after treatment with GM-CSF (30 microgram/day)compared with the number of patients pregnant in the control group

Secondary

MeasureTime frameDescription
implantation rate12 monthsnumber of embryos implanted

Countries

Italy

Contacts

Primary ContactMarco Sbracia, MD
marcandrea@hotmail.com+393479037433
Backup ContactFabio Scarpellini, MD
marcandrea@hotmail.com+393278779064

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026