- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03635346
Medicinal Dependence and Chronic Pain: Addictive Evaluation in CETD (DEMDOU)
August 16, 2018 updated by: University Hospital, Brest
prescription opioid misuse in chronic pain is a growing public health concern. few studies got interested in prevalence of misuse and of opiate use disorder in a population of patients with a non cancer chronic pain.
the investigators analyzed during 3 months opiate misuse and opiate ude disorder in a population of patients consulting a center specialized in pain management.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
128
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Brest, France, 29609
- CHRU de Brest
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
analysis of SUD criteria in a population with a chronic pain (non cancer) , consulting a center specialized in pain mangement
Description
Inclusion Criteria:
- patient with a non cancer chronic pain
- consulting a CETD center
Exclusion Criteria:
- non understanding of french
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
DSM 5 criteria of SUD
Time Frame: Day 0 (at the inclusion)
|
11 criteria of SUD
|
Day 0 (at the inclusion)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 3, 2016
Primary Completion (Actual)
September 3, 2016
Study Completion (Actual)
March 10, 2018
Study Registration Dates
First Submitted
August 14, 2018
First Submitted That Met QC Criteria
August 16, 2018
First Posted (Actual)
August 17, 2018
Study Record Updates
Last Update Posted (Actual)
August 17, 2018
Last Update Submitted That Met QC Criteria
August 16, 2018
Last Verified
July 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DEMDOU 2016.CE13
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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