The main objective of this study is to estimate the reporting bias of patients in terms of
prescripted drug and care consumption by comparing data collected in a patient diary and
database of health insurance .
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Full eligibility criteria for NCT02893059
Ages eligible for Study
18 Years to 75 Years
Genders eligible for Study
Accepts Healthy Volunteers
incident and prevalent cases of patients with type I or type II diabetes. arthritis:
incident and prevalent cases of rheumatoid arthritis patients defined according to the ACR-EULAR criteria 2010 (Aletaha D et al, 2010). Renal failure :
• incident and prevalent cases of patients with kidney disease stage 3 or 4, transplanted or not. Prostate cancer :
• Incident cases of patients with prostate cancer regardless of the stage at diagnosis
(positive prostate biopsy). Breast cancer :
• Incident cases of patients with breast cancer regardless of the stage at diagnosis
(biopsy positive breast). Colorectal cancer :
• Incident cases of patients with colorectal cancer regardless of the stage at diagnosis
(colonoscopy and polyp biopsy positive).
The subject participates in an experimental study of research affecting the therapeutic management of the patient.
The subject is exclusion period determined by a previous study.
The subject is under judicial protection, guardianship or curatorship.
It is not possible to give informed about information
The subject does not read French and is not autonomous filling a questionnaire.
The patient has psychiatric disorders.
The subject is an emergency.
Monitoring between patient visits than 6 months.
All locations for NCT02893059
View full eligibility
Tris trial is registered with FDA with number: NCT02893059. The sponsor of the trial is Centre Hospitalier Universitaire de Nīmes and it is looking for 300 volunteers for the current phase.
Official trial title: Evaluation of a Data Collection Tool in Clinical Research: Comparison Between the Data Collected by Patient Diary and Data From Medical Administrative Databases
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