EmbryoGen/ Blastgen for Couples With Implantation Problems or Previous Miscarriage (BlastGen)
Primary Purpose
Recurrent Miscarriage, Infertility
Status
Completed
Phase
Phase 4
Locations
Australia
Study Type
Interventional
Intervention
EmbryoGen/ BlastGen media
Standard Cook sequential media
Sponsored by
About this trial
This is an interventional treatment trial for Recurrent Miscarriage
Eligibility Criteria
Inclusion Criteria:
women undertaking an IVF or ICSI cycle
- aged between 25 and 41 years
- 2 or more embryos transferred without a positive pregnancy outcome OR a history of at least 1 previous pregnancy loss, OR
- Poor embryo development (<20% of embryo developing on time at Day 3 or no blastocyst above Grade 2 on Day 5)
Exclusion Criteria:
- male partner requiring surgical retrieval of sperm except in cases of previous vasectomy
- the use of another investigational drug within 30 days
- any severe chronic disease that would significantly influence an IVF cycle
- less than 3 follicles>14mm on ultrasound on the day of HCG trigger
Sites / Locations
- FertilitySA
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
EmbryoGen/BlastGen
Control
Arm Description
EmbryoGen and BlasGen media containing GM-CSF 2ng/ml will be used in the experimental arm The intervention is to use EmbryoGen/BlastGen
Standard Cook sequential media
Outcomes
Primary Outcome Measures
Livebirth >20 weeks
Any delivery >20 resulting in a livebirth
Secondary Outcome Measures
Congenital Anomaly Rate
number of liveborns with a congenital anomaly
Clinical pregnancy rates at 7 and 12 weeks gestation
Fetal Heart Beat seen on Ultrasound scan at 7 and 12 weeks
Number of embryos reaching blastocyst stage
Number of blastocysts per cycle
Day 3 and day 5 embryo scores
grade of day 3 and day 5 embryos
Cryopreservation outcomes
Number of Frozen blastocysts
Full Information
NCT ID
NCT02305420
First Posted
November 27, 2014
Last Updated
February 14, 2018
Sponsor
FertilitySA
Collaborators
University of Adelaide
1. Study Identification
Unique Protocol Identification Number
NCT02305420
Brief Title
EmbryoGen/ Blastgen for Couples With Implantation Problems or Previous Miscarriage
Acronym
BlastGen
Official Title
EmbryoGen/ Blastgen for Couples With Implantation Problems or Previous Miscarriage
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
November 2014 (Actual)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
June 14, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
FertilitySA
Collaborators
University of Adelaide
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
EmbryoGen and BlastGen contain the cytokine growth factor Granulocyte-Macrophage Colony-Stimulating Factor (GM-CSF), which has been documented to give significant benefit to this difficult group of patients.
Results showed a highly significant effect of 44% relative improvement in ongoing implantation rate (p=0.001) in women who have previously miscarried (Ziebe et al 2013).
We wish to undertake a randomised Controlled trial to determine if EmbryoGen/BlastGen media improves pregnancy outcomes in women with recurrent implantation failure, recurrent miscarriage and poor embryo development when compared to standard media.
Detailed Description
A randomised control pilot study will be undertaken for 100 women who have implantation failure (≥ 2 embryo transfers without a pregnancy) or at least 1 previous miscarriage and are having a further IVF cycle.
At oocyte retrieval each couple will be randomised using numbered envelopes containing pre randomised group allocations by a person uninvolved in the trial to:
BlastGen Group (n=50): culturing their embryos in ORIGIO standard, sequential culture mediums for 3 days (EmbryoGen included) then BlastGen media (GM-CSF containing media) for remaining 2 days or
Standard Media Group (n=50): culturing their embryos in Cook standard sequential medium for 5 days.
The best single embryo will be transferred on day 5.
The clinical staff and participating couple will be blinded as to whether BlastGen or standard media was used in culture to day 5. Fertility SA embryologists will not be blind as to which study group a couple is in and which media is being used. The embryos will be cultured using the usual methods and lab facilities by Fertility SA's current embryology staff members who will not be blind to the media being used.
Records on the outcome of the oocyte fertilisation, blastocyst development, implantation rate and pregnancy rates will be recorded, as is standard practice. Pregnancy scans will be carried out at 7 and 12 weeks. Live birth outcomes and any congenital anomalies will be recorded.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Miscarriage, Infertility
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
Randomised control trial comparing EmbryoGen/ BlastGen media use with standard media in IVF
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EmbryoGen/BlastGen
Arm Type
Experimental
Arm Description
EmbryoGen and BlasGen media containing GM-CSF 2ng/ml will be used in the experimental arm
The intervention is to use EmbryoGen/BlastGen
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Standard Cook sequential media
Intervention Type
Device
Intervention Name(s)
EmbryoGen/ BlastGen media
Other Intervention Name(s)
GM-CSF containing media
Intervention Description
Embryos will be cultured in media containing Gm-CSF (EmbryoGen/ BlastGen media)
Intervention Type
Device
Intervention Name(s)
Standard Cook sequential media
Intervention Description
Standard Cook IVF media will be used in the control arm
Primary Outcome Measure Information:
Title
Livebirth >20 weeks
Description
Any delivery >20 resulting in a livebirth
Time Frame
9 months after closure of trial (18 +9 months)
Secondary Outcome Measure Information:
Title
Congenital Anomaly Rate
Description
number of liveborns with a congenital anomaly
Time Frame
9 months after closure of trial (18 +9 months)
Title
Clinical pregnancy rates at 7 and 12 weeks gestation
Description
Fetal Heart Beat seen on Ultrasound scan at 7 and 12 weeks
Time Frame
18 months
Title
Number of embryos reaching blastocyst stage
Description
Number of blastocysts per cycle
Time Frame
18 months
Title
Day 3 and day 5 embryo scores
Description
grade of day 3 and day 5 embryos
Time Frame
18 months
Title
Cryopreservation outcomes
Description
Number of Frozen blastocysts
Time Frame
18 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
41 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
women undertaking an IVF or ICSI cycle
aged between 25 and 41 years
2 or more embryos transferred without a positive pregnancy outcome OR a history of at least 1 previous pregnancy loss, OR
Poor embryo development (<20% of embryo developing on time at Day 3 or no blastocyst above Grade 2 on Day 5)
Exclusion Criteria:
male partner requiring surgical retrieval of sperm except in cases of previous vasectomy
the use of another investigational drug within 30 days
any severe chronic disease that would significantly influence an IVF cycle
less than 3 follicles>14mm on ultrasound on the day of HCG trigger
Facility Information:
Facility Name
FertilitySA
City
Adelaide
State/Province
South Australia
ZIP/Postal Code
5006
Country
Australia
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32220517
Citation
Rose RD, Barry MF, Dunstan EV, Yuen SM, Cameron LP, Knight EJ, Norman RJ, Hull ML. The BlastGen study: a randomized controlled trial of blastocyst media supplemented with granulocyte-macrophage colony-stimulating factor. Reprod Biomed Online. 2020 May;40(5):645-652. doi: 10.1016/j.rbmo.2020.01.011. Epub 2020 Jan 23.
Results Reference
derived
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EmbryoGen/ Blastgen for Couples With Implantation Problems or Previous Miscarriage
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