se of MEOPA by elderly with dementia

• Conditions: PAIN DUE TO BEDSORE OR WOUND BY ELDERLY WITH DEMENTIA; MedDRA version: 9.1Level: LLTClassification code 10056350Term: Pain management

• Registration Number: EUCTR2008-000239-17-FR
• Lead Sponsor: CHU de NICE

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2008-04-10
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

PATIENTS OLDER THAN 75
DIAGNOSTIC OF DEMENTIA
NECESSITY OF PAIN MANAGEMENT
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) no
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

CHANGE OF MEDICATION OR ANALGESIC < 24 HOURS

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main Objective: ASSESSMENT OF USE OF MEOPA BY ELDERLY WITH DEMENTIA AS A SUBSTITUTION OF USE OF OPIODS DURING PAINFULL CARE ;Secondary Objective: DESCRIPTION OF SECONDARY EFFECTS<br>SATISFACTION ASSESSMENT OF PATIENTS AND NURSE<br>STUDY OF ASSOCIATION BETWEEN TOLERANCE TO MEOPA AND DEGREE OF DEMENTIA;Primary end point(s): PAIN ASSESSMENT<br>SATISFACTION OF PATIENTS AND NURSE