Trial record 8 of 482 for:    "tetrasomy 18p" OR "Chromosomal Disorder"

Chromosomal Analysis of Single Cells in Human Embryos

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2008 by Katholieke Universiteit Leuven.
Recruitment status was  Active, not recruiting
Sponsor:
Information provided by:
Katholieke Universiteit Leuven
ClinicalTrials.gov Identifier:
NCT00614367
First received: January 30, 2008
Last updated: February 11, 2008
Last verified: January 2008
  Purpose

Optimise genetic screening of human embryos using higher resolution techniques


Condition
Chromosomal Abnormalities

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Chromosomal Analysis of Single Cells in Human Embryos

Resource links provided by NLM:


Further study details as provided by Katholieke Universiteit Leuven:

Primary Outcome Measures:
  • genetic constitution of single blastomeres [ Time Frame: 3 day old embryos ] [ Designated as safety issue: No ]

Biospecimen Retention:   Samples With DNA

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)
  Eligibility

Ages Eligible for Study:   up to 4 Days
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population

3-4 day old human IVF embryos

Criteria

Inclusion Criteria:

  • 3-4 day old embryos from IVF couples with both partners younger than 36 years old
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00614367

Locations
Belgium
University Hospital Leuven, Catholic University Leuven
Leuven, Belgium, 3000
Sponsors and Collaborators
Katholieke Universiteit Leuven
Investigators
Principal Investigator: Joris Vermeesch, Prof PhD University Hospital Leuven, Catholic University Leuven
Study Director: Thomas D'hooghe, Prof MD PhD Universitaire Ziekenhuizen Leuven
  More Information

No publications provided

Responsible Party: Prof Joris Vermeesch, University Hospital Leuven - Catholic University Leuven
ClinicalTrials.gov Identifier: NCT00614367     History of Changes
Other Study ID Numbers: ML4102005
Study First Received: January 30, 2008
Last Updated: February 11, 2008
Health Authority: Belgium: Institutional Review Board

Keywords provided by Katholieke Universiteit Leuven:
chromosomal abnormalities in single cells

Additional relevant MeSH terms:
Congenital Abnormalities
Chromosome Aberrations
Chromosome Disorders
Pathologic Processes
Genetic Diseases, Inborn

ClinicalTrials.gov processed this record on April 22, 2014