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CompletedNCT02305420

EmbryoGen/ Blastgen for Couples With Implantation Problems or Previous Miscarriage

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (actual)
Sponsor
FertilitySA · Industry
Sex
Female
Age
25 Years – 41 Years
Healthy volunteers
Not accepted

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: 1. 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 2. 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.

Conditions

Interventions

TypeNameDescription
DEVICEEmbryoGen/ BlastGen mediaEmbryos will be cultured in media containing Gm-CSF (EmbryoGen/ BlastGen media)
DEVICEStandard Cook sequential mediaStandard Cook IVF media will be used in the control arm

Timeline

Start date
2014-11-01
Primary completion
2017-06-01
Completion
2017-06-14
First posted
2014-12-02
Last updated
2018-02-19

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT02305420. Inclusion in this directory is not an endorsement.