Impact of a Personalized Medication Plan on Duration of Treatment With Potent Opioids in Acute Non-cancer Musculoskeletal Pain.
Condition(s) studied
Investigational drug(s) / intervention(s)
personalized pharmaceutical plan: multi-professional intervention around strong opioid treatment with targeted pharmaceutical interview
Study summary
The aim of this study is to evaluate whether patients who benefit from a personalized pharmaceutical plan (PPP) during their hospitalization, allowing them to be informed and sensitized, are treated for a shorter period of time with strong opioids with a reduced risk of dependence compared to a management according to the usual modalities in the rheumatology services concerned.
Eligibility
Primary outcome measure(s)
- total duration of treatment in days with strong opioids from day of inclusion — 6 months
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU de Lille | Lille | France | Recruiting |
| CHU de Nimes | Nîmes | France | Recruiting |
| CHU de ROUEN | Rouen | France | Recruiting |
More University Hospital, Rouen trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05905146 on ClinicalTrials.gov ↗ ← All trials in France