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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03736070
Other study ID # RECHMPL18_0069
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2018
Est. completion date December 1, 2021

Study information

Verified date June 2020
Source University Hospital, Montpellier
Contact Claire M DUFLOS, MD
Phone 467336407
Email c-duflos@chu-montpellier.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In 2018, 10 detention centers in France will start organisational programs to improve the quality of screening of oral diseases, relatively to French recommendations, among new prisoners in France. Our study aims 1) to assess the prevalence and nosology of oral diseases ; 2) to describe the care pathway of participants during their stay in the detention center where they were included ; 3) to assess the cost of care per patient, from a societal perspective, using a top-down method.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 1, 2021
Est. primary completion date May 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria:

- new prisoners

- fluent French language

Exclusion criteria:

- adult guardianship

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Montpellier General Health Office, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Description of the oral problems of people entering detention Description of the oral problems of people entering detention : Any oral disease at inclusion (prevalence study) 1 day
Secondary attending to consultations attending to consultations : The rate of attended visits is defined as the number of visits attended by the patient, divided by the number of scheduled visits, during the prison stay of the participant. The collection of data will end at the discharge of the participant, or at 6 months after inclusion.
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