Use of GM-CSF Treatment in Recurrent Implantation Failure
Primary Purpose
Women With Recurrent Implantation Failure in IVF
Status
Recruiting
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
GM-CSF group
CONTROL
Sponsored by
About this trial
This is an interventional treatment trial for Women With Recurrent Implantation Failure in IVF focused on measuring GM-CSF, IVF failure,pregnancy
Eligibility Criteria
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.)
Sites / Locations
- Cerm-HungariaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
CONTROL
GM-CSF group
Arm Description
patients with recurrent implantation failure treated with PLACEBO (saline solution) from the day of embryo transfer through the day of beta hCG test
patients with recurrent implantation failure treated with GM-CSF (30 micrograms/day) from the day of embryo transfer through the day of beta hCG test
Outcomes
Primary Outcome Measures
pregnancy outcome
The number of patients pregnant after treatment with GM-CSF (30 microgram/day)compared with the number of patients pregnant in the control group
Secondary Outcome Measures
implantation rate
number of embryos implanted
Full Information
NCT ID
NCT01715974
First Posted
March 2, 2012
Last Updated
July 18, 2022
Sponsor
Centre for Endocrinology and Reproductive Medicine, Italy
1. Study Identification
Unique Protocol Identification Number
NCT01715974
Brief Title
Use of GM-CSF Treatment in Recurrent Implantation Failure
Official Title
Administration of GM-CSF in Women With Recurrent Implantation Failure in IVF Cycles and Egg Donation Cycles
Study Type
Interventional
2. Study Status
Record Verification Date
July 2022
Overall Recruitment Status
Recruiting
Study Start Date
December 12, 2017 (Actual)
Primary Completion Date
July 31, 2022 (Anticipated)
Study Completion Date
August 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre for Endocrinology and Reproductive Medicine, Italy
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Women With Recurrent Implantation Failure in IVF
Keywords
GM-CSF, IVF failure,pregnancy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
140 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CONTROL
Arm Type
Placebo Comparator
Arm Description
patients with recurrent implantation failure treated with PLACEBO (saline solution) from the day of embryo transfer through the day of beta hCG test
Arm Title
GM-CSF group
Arm Type
Experimental
Arm Description
patients with recurrent implantation failure treated with GM-CSF (30 micrograms/day) from the day of embryo transfer through the day of beta hCG test
Intervention Type
Drug
Intervention Name(s)
GM-CSF group
Other Intervention Name(s)
GM-CSF
Intervention Description
30 micrograms/day of GM-CSF from the day of embryo transfer through the day of beta HCG test
Intervention Type
Drug
Intervention Name(s)
CONTROL
Other Intervention Name(s)
SALINE INFUSION
Intervention Description
saline infusion every day from the day of embryo transfer through the day of beta HCG test
Primary Outcome Measure Information:
Title
pregnancy outcome
Description
The number of patients pregnant after treatment with GM-CSF (30 microgram/day)compared with the number of patients pregnant in the control group
Time Frame
12 months
Secondary Outcome Measure Information:
Title
implantation rate
Description
number of embryos implanted
Time Frame
12 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marco Sbracia, MD
Phone
+393479037433
Email
marcandrea@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Fabio Scarpellini, MD
Phone
+393278779064
Email
marcandrea@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marco Sbracia, MD
Organizational Affiliation
Centre for Endocrinology and Reproductive Medicine, Italy
Official's Role
Study Chair
Facility Information:
Facility Name
Cerm-Hungaria
City
Rome
ZIP/Postal Code
198
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marco Sbracia, MD
Phone
+393479037433
Email
marcandrea@hotmail.com
First Name & Middle Initial & Last Name & Degree
Fabio Scarpellini, MD
Phone
+393278779064
Email
marcandrea@hotmail.com
12. IPD Sharing Statement
Citations:
PubMed Identifier
19617208
Citation
Scarpellini F, Sbracia M. Use of granulocyte colony-stimulating factor for the treatment of unexplained recurrent miscarriage: a randomised controlled trial. Hum Reprod. 2009 Nov;24(11):2703-8. doi: 10.1093/humrep/dep240. Epub 2009 Jul 17.
Results Reference
background
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Use of GM-CSF Treatment in Recurrent Implantation Failure
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