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Sponsored by: |
Katholieke Universiteit Leuven |
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Information provided by: | Katholieke Universiteit Leuven |
ClinicalTrials.gov Identifier: | NCT00614367 |
Optimise genetic screening of human embryos using higher resolution techniques
Condition |
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Chromosomal Abnormalities |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | Chromosomal Analysis of Single Cells in Human Embryos |
Single blastomeres of human embryos
Enrollment: | 30 |
Study Start Date: | October 2005 |
Estimated Study Completion Date: | June 2008 |
Estimated Primary Completion Date: | March 2008 (Final data collection date for primary outcome measure) |
Ages Eligible for Study: | up to 4 Days |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Probability Sample |
3-4 day old human IVF embryos
Inclusion Criteria:
Belgium | |
University Hospital Leuven, Catholic University Leuven | |
Leuven, Belgium, 3000 |
Principal Investigator: | Joris Vermeesch, Prof PhD | University Hospital Leuven, Catholic University Leuven |
Study Director: | Thomas D'hooghe, Prof MD PhD | University Hospital Leuven |
Responsible Party: | University Hospital Leuven - Catholic University Leuven ( Prof Joris Vermeesch ) |
Study ID Numbers: | ML4102005 |
Study First Received: | January 30, 2008 |
Last Updated: | February 11, 2008 |
ClinicalTrials.gov Identifier: | NCT00614367 |
Health Authority: | Belgium: Institutional Review Board |
chromosomal abnormalities in single cells |
Chromosomal abnormalities Genetic Diseases, Inborn Chromosome Aberrations Chromosome Disorders Congenital Abnormalities |
Pathologic Processes |