Effect of patient-controlled sedation with propofol on patient satisfactio

Completed

• Conditions: Diagnostic cerebral angiography; Signs and Symptoms

• Registration Number: ISRCTN81377748
• Lead Sponsor: Assistance Publique ? Hôpitaux de Marseille AP-HM (France)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-04-16
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

1. Age under 70 years
2. ASA physical status below 3
3. Scheduled cerebral angiography
4. Consultation with an anesthetist at least 48 hours before the procedure

Exclusion Criteria

1. Age under 18 years,
2. Emergency context
3. History of psychiatric disease
4, Long-course anxiolytic treatment
5. Counter-indication to propofol
6. Withdrawal of consent

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The main objective was to evaluate whether a propofol-based PCS would lead at least to 20% difference in patients? satisfaction on the EVAN scale, which was self reported the day after the procedure.

Secondary Outcome Measures

Name	Time	Method
Secondary objectives were to assess the quality of patient conditioning by the neuroradiologist and the anesthetist and to report possible side effect.