Actively Recruiting
Impact of a Personalized Medication Plan on Duration of Treatment With Potent Opioids in Acute Non-cancer Musculoskeletal Pain.
Led by University Hospital, Rouen · Updated on 2026-02-06
200
Participants Needed
3
Research Sites
234 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Impact of a Personalized Medication Plan on Duration of Treatment With Potent Opioids in Acute Non-cancer Musculoskeletal Pain.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient hospitalized in the rheumatology department
- Acute pain due to non-cancerous, non-traumatic, high-energy musculoskeletal pathology
- Prescription of strong opioid derivatives started in rheumatology or maintained if initial prescription lasted no more than 30 consecutive days before inclusion
You will not qualify if you...
- Diagnosed with cancer or fibromyalgia at inclusion
- Poor French language skills
- Taking strong opioid treatment for more than 30 consecutive days before inclusion
- Judged not autonomous for managing strong opioid treatment by prescriber or pharmacist
- Already included in the study
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 3 locations
1
CHU de Lille
Lille, France
Actively Recruiting
2
CHU de Nimes
Nîmes, France
Actively Recruiting
3
CHU de ROUEN
Rouen, France
Actively Recruiting
Research Team
C
Catherine CHENAILLER
CONTACT
A
Armelle GUIDOTTI
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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