Intra- and Interobserver Agreement in the Assessment of Human Embryos
NCT ID: NCT01802801
Last Updated: 2013-03-01
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.
COMPLETED
50 participants
OBSERVATIONAL
2007-12-31
2009-08-31
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.
International Pilot Study for Dual Non-invasive Assesment of Embryo Development
NCT06524648
Genetic Screening and Assisted Oocyte Activation in Couples with Diminished/aberrant Embryonic Development.
NCT03354013
Embryo Selection Using Non-invasive Metabolomic Analysis Versus Morphology
NCT01490515
Morphometrics and Morphokinetics of Thawed Oocytes and Embryos
NCT02639715
Impact of Culture Conditions on the Embryo Quality
NCT01767805
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 Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
embryo development
intra- and inter-observator analysis
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
embryo development
intra- and inter-observator analysis
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
1 Day
3 Days
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Gasthuisberg
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Thomas D'Hooghe
Prof. Dr.
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.
GP12122007
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.