Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
30 participants
OBSERVATIONAL
2005-10-31
2008-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Genome-wide Single Cell Haplotyping as a Generic Method for Preimplantation Genetic Diagnosis
NCT01336400
Pre-Implantation Genetic Screening in Women Under the Age of 36 Years With Single Embryo Transfer
NCT00670059
Genetic Screening and Assisted Oocyte Activation in Couples with Diminished/aberrant Embryonic Development.
NCT03354013
Study of Late-foetal Human Organ Development
NCT04661059
Preimplantation Genetic Screening in Women Over 35 Year
NCT00593671
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
3 Days
4 Days
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
KU Leuven
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
University Hospital Leuven - Catholic University Leuven
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Joris Vermeesch, Prof PhD
Role: PRINCIPAL_INVESTIGATOR
University Hospital Leuven, Catholic University Leuven
Thomas D'hooghe, Prof MD PhD
Role: STUDY_DIRECTOR
Universitaire Ziekenhuizen KU Leuven
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Hospital Leuven, Catholic University Leuven
Leuven, , Belgium
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ML4102005
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.