Big Data Analysis of the Use of bIomarkers Concentration
rUBIDIuM
Defining Use and Misuse of BIoMarkers Dosage and Trends in Observed Concentration Over Time: a BIg Data Analysis
1 other identifier
observational
585,745
1 country
1
Brief Summary
The investigators conducted a retrospective analysis of all measured concentrations performed in a large subset of laboratories located in the French Brittany from February 2010 the 17th to August 2015 the 30th, in adults over 20 years old. The investigators are aimed at studying physicians' use and eventually misuse of biomarkers dosage and the characteristics of a broad population based on some biomarkers concentrations.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2010
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 17, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 30, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
September 10, 2015
CompletedFirst Submitted
Initial submission to the registry
August 16, 2017
CompletedFirst Posted
Study publicly available on registry
August 18, 2017
CompletedAugust 22, 2017
August 1, 2017
5.5 years
August 16, 2017
August 18, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
biomarker dosage prescription
physicians' use and eventually misuse of biomarkers dosage
August 2017
Secondary Outcomes (3)
Biomarkers dosage numbers
August 2017
Biomarkers in geriatric patients
August 2017
Population's characteristics
August 2017
Interventions
Eligibility Criteria
Cohort that included all analyses performed in a large subset of laboratories located in the French Brittany from February 2010 the 17th to August 2015 the 30th. The extract data corresponded to 74,502,510 analyses performed in 585,745 distinct adult patients \>20y
You may qualify if:
- All adult patients \>20 that came to a participating lab (Biorance Laboratoires Réunis) during the study period for biological measurement
You may not qualify if:
- DNA analysis, HIV test
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Hospital Avicennelead
- Roche Diagnostics GmbHcollaborator
- ProBayescollaborator
- Biorance Laboratoires Réuniscollaborator
Study Sites (1)
Avicenne Hospital
Bobigny, 93000, France
Study Officials
- PRINCIPAL INVESTIGATOR
Christophe Meune, MD PhD
Avicenne Hospital
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 16, 2017
First Posted
August 18, 2017
Study Start
February 17, 2010
Primary Completion
August 30, 2015
Study Completion
September 10, 2015
Last Updated
August 22, 2017
Record last verified: 2017-08
Data Sharing
- IPD Sharing
- Will not share
Only aggregated data are available