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Completed

NCT Number: NCT03254472

Big Data Analysis of the Use of bIomarkers Concentration

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.

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Avicenne Hospital

Bobigny, 93000, France

About this study

The rUBIDIuM study is a retrospective analysis that included all tests (but not including DNA analysis or HIV tests) performed in a large subset of laboratories located in the French Brittany from February 2010 the 17th to August 2015 the 30th. The area of study covers most of the Ille-et-Vilaine and a part of the Côtes d'Armor department in Brittany. The respective surface of these departments is 6775 and 6878 km2. All labs belong to the Biorance Laboratory group (consortium of 33 labs, Biorance Laboratoires Réunis) and are equipped with Roche Diagnostics instruments (Elecsys2010® analyzer, Roche diagnostics, Meylan, France).

The main objectives are to study physicians' use and eventually misuse of biomarkers dosage and the characteristics of this broad population based on some biomarkers concentrations.

For all adult patients >20y that came to a participating lab during the study period, the investigators collected the following information: demographics data, data about the prescription (date of order, list of analysis recommended, the date of blood collection and analysis), about the prescribers and the results of the analyses. After a de-identifying process, data were aggregated.

the initial analyses will 1) examine the biological tests (number, types…) ordered in a large cohort of patients, in the total population and the subgroups based on gender, age, time period, kind of lab and physicians' specialty, 2) examine the results/concentration of the analyses: blood chemistry, creatinin concentration, cardiac enzymes, natriuretic peptides, INR, lipid profile, hemogram…

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All adult patients >20 that came to a participating lab (Biorance Laboratoires Réunis) during the study period for biological measurement

Exclusion criteria

  • DNA analysis, HIV test

Treatment and study plan

Measured concentrations of biomarkers

Diagnostic Test

Primary outcomes

  1. biomarker dosage prescription

    Time frame: August 2017

    physicians' use and eventually misuse of biomarkers dosage

Secondary outcomes

  1. Biomarkers dosage numbers

    Time frame: August 2017

    Biomarkers dosage numbers before and after new treatments, released of guidelines, new tests...

  2. Biomarkers in geriatric patients

    Time frame: August 2017

    biomarkers dosages and concentration in elderly/very elderly patients

  3. Population's characteristics

    Time frame: August 2017

    physicians' use and eventually misuse of biomarkers dosage

Sponsors and collaborators

Lead sponsor

Hospital Avicenne

Other

Collaborators

  • Biorance Laboratoires Réunis
  • ProBayes
  • Roche Diagnostics GmbH

Registry information

Official study title

Defining Use and Misuse of BIoMarkers Dosage and Trends in Observed Concentration Over Time: a BIg Data Analysis

Acronym: rUBIDIuM

Important dates

Study start
2010
Primary completion
2015
Study completion
2015
First posted
Aug 18, 2017
Registry last updated
Aug 22, 2017

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.

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