Completed

Intra-and Inter-observer Agreement in the Morphological Assessment of Human Embryos

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being collected

Data Collection

Other
Who is being recruted

+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Observational
Study Start: December 2007
See protocol details

Summary

Principal SponsorUniversity Hospital, Gasthuisberg
Last updated: March 1, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 2007

Actual date on which the first participant was enrolled.

The purpose of this study is to determine the intra- and interobserver agreement.

NCT01802801
Principal SponsorUniversity Hospital, Gasthuisberg
Last updated: March 1, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

50 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

1 inclusion criteria required to participate
fertilized embryos
1 exclusion criteria prevent from participating
unfertilized embryos

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

University Hospital Leuven, Catholic University Leuven

Leuven, BelgiumOpen University Hospital Leuven, Catholic University Leuven in Google Maps
CompletedOne Study Center