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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT03390829
Other study ID # 2017-A01752-51
Secondary ID
Status Enrolling by invitation
Phase N/A
First received October 19, 2017
Last updated December 29, 2017
Start date October 20, 2017
Est. completion date April 20, 2019

Study information

Verified date October 2017
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Consultations in general medical practice concerning the follow-up of the patients receiving opiate substitution treatments are not exceptional.

It is nowadays agreed that addictive pathology goes far beyond the issue of product dependence, in favor of a pathology in itself. Centered on problems of attachment, of framework, of trust. The implementation of the opiate substitution treatments and the lifting of the product dependence appears only as a preliminary to the background work with the patient ex-user of opiate.

Finally, the literature provides little information on the experience of general practitioners and their patients under opiate substitution treatments regarding follow-up consultations in the stability phase.

The objective of this work is therefore to study the feelings on follow-up consultations, general practitioners and their patients under opiate substitution treatments considered stabilized.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 20
Est. completion date April 20, 2019
Est. primary completion date April 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- major people patients receiving opiate substitution treatments

Exclusion Criteria:

- considered unstabilized with opiate substitution treatments

Study Design


Related Conditions & MeSH terms


Intervention

Other:
semi-directed interviews
semi-directed interviews

Locations

Country Name City State
France Université Angers Angers

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary assessment of feelings on follow-up consultations with standardized questionnaire 1 hour
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