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Diagnostic efficiency and accuracy, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis.

Diagnostic efficiency and accuracy, embryonic development and clinical outcome after the biopsy of one or two blastomeres for preimplantation genetic diagnosis.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON24785
Enrollment
592
Registered
2007-02-27
Start date
2001-01-05
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

1. Preimplantation genetic diagnosis (NLD: preimplantatie genetische diagnose)

Interventions

Embryos were obtained from patients undergoing PGD. One or two cells were removed from embryos with more than 6 cells at day 3. Embryos shown to be free of disease were replaced in the uterus. Some s

Sponsors

Centrum Medische Genetica en Centrum Reproductieve Geneeskunde, Universitair Ziekenhuis Brussel Vakgroep Embryologie en Genetica, Vrije Universiteit Brussel
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: PGD cycles for monogenic diseases, sexing or screening in which one or two cells can be removed from the embryos.

Exclusion criteria

Exclusion criteria: PGD where two cells must be removed for accurate diagnosis: monogenic cycles where PCR for one locus is carried out, or PGD for translocation carriers.

Design outcomes

Primary

MeasureTime frame
1. Embryo transfer rate; 2. Positive hCG; 3. Implantation rate; 4. Live birth rate.

Secondary

MeasureTime frame
1. In-vitro embryonic development after the removal of one or two blastomeres; 2. The diagnostic efficiency of both PCR- and FISH techniques for PGD.

Contacts

Public ContactKaren Sermon

Centre for Medical Genetics, UZ Brussel, Laarbeeklaan 101

karen.sermon@uzbrussel.be+32 2 477 60 73

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)