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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03297853
Other study ID # RECHMPL17_0305
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2014
Est. completion date March 30, 2018

Study information

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

Clinical Trial Summary

The demand for addiction care for patients with addiction to analgesics increases with the number of prescription of analgesics grade 2; this is a public health problem There is no support for repositories to date in the context of addiction analgesics grade 2.

Risk factors of misuse as well as diagnostic tools were identified.


Description:

The demand for addiction care for patients with addiction to analgesics increases with the number of prescription of analgesics grade 2; this is a public health problem There is no support for repositories to date in the context of addiction analgesics grade 2.

Risk factors of misuse as well as diagnostic tools were identified. The objectives of our research are to determine the characteristics of the individuals suffering from an addiction to analgesics of level 2 followed in consultation of addictology in the hospital of Montpellier and Nimes and to describe the type of follow-up proposed to the patients in these two centers. It is a retrospective and descriptive study.

As part of this research, we will solicit all the patients followed in consultation of addictology or in hospitalization to the hospital of Montpellier or Nîmes for an addiction to the analgesics of grade 2 between the 1st of January 2014 and the 10th of July 2017 with requests of management for withdrawal or reduction of doses, opioid analgesics in the absence of pain or in chronic non-cancer pain, opioid analgesics to avoid withdrawal syndrome or hyperalgesia and consumptions chronic to dosages inadequate to the functional complaint evaluated by the rhumatology or algology services.

The data are collected in the medical file at the two participating institutions (Montpellier and Nîmes) and if necessary, patients not seen in consultation for more than 6 months will be recontacted.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date March 30, 2018
Est. primary completion date July 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Requests for management for weaning or reduction of doses

- Take opioid analgesics in the absence of pain or as part of chronic non-cancer pain

- Opioid analgesics to prevent withdrawal syndrome or hyperalgesia

- Chronic consumption at inadequate dosages compared to the functional complaint evaluated by the MPR / Algologie services

- Patients over 18 years and who agree with the study

Exclusion criteria:

- language barrier

- severe cognitive and / or psychiatric disorders

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary 50/5000 Prevalence of demand for care in addictology Prevalence of demand for addictive care in subjects with addiction to analgesics in level 2 1 day
Secondary Types of support proposed Types of support proposed 1 day
Secondary Assessment of analgesic dependence Assessment of analgesic dependence 1 day
Secondary History of analgesic use History of analgesic use 1 day
Secondary quality of life quality of life 1 day