University Hospital Leuven, Catholic University Leuven
Leuven, Belgium
Completed
NCT Number: NCT01802801
Intra- and Interobserver Agreement in the Assessment of Human Embryos
The purpose of this study is to determine the intra- and interobserver agreement.
Completed
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Notify MeKey information
Age range
1 day–3 day
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- fertilized embryos
Exclusion criteria
- unfertilized embryos
Treatment and study plan
embryo development
Otherintra- and inter-observator analysis
Primary outcomes
-
Evaluation of the intra- and inter-observer variability in the assessement of human embryos
Variation in observer assessment of embryo characteristics on day 1, 2 and 3 of embryo development. Assessment of these characteristics is standard procedure. Safety and tolerability or efficacy issues are not relevant for this outcome.
Sponsors and collaborators
Lead sponsor
University Hospital, Gasthuisberg
Other
Registry information
Official study title
Intra-and Inter-observer Agreement in the Morphological Assessment of Human Embryos
Important dates
- Study start
- 2007
- Primary completion
- 2009
- Study completion
- 2009
- First posted
- Mar 1, 2013
- Registry last updated
- Mar 1, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.