Clinical Research and Data Collection During the Investigation: Influence of a Dedicated Staff

NCT03946501 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2019-05-10

No results posted yet for this study

Summary

The aim of the study was to evaluate the interest of the recourse of a staff dedicated as CRA to data collection in clinical research

Conditions

  • Clinical Research Inclusion

Interventions

OTHER

Data collection

Sponsors & Collaborators

  • CHU de Reims

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-03-01
Primary Completion
2015-04-01
Completion
2015-05-01

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03946501 on ClinicalTrials.gov