Pain assessment during general anesthesia : DOLANS Study - DOLANS

• Conditions: perioperative analgesia; MedDRA version: 12.1Level: LLTClassification code 10054799Term: Perioperative analgesia

• Registration Number: EUCTR2010-019591-67-FR
• Lead Sponsor: CHU de SAINT-ETIENNE

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2010-05-06
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

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

Inclusion Criteria

18 to 55 years old
ASA status 1 or 2
Patients scheduled to undergo general anesthesia for different types of surgery (neurosurgical or medular surgery, ear, nose or throat surgery or orthopedic surgery)
Gived informed consent before the study
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

patient admit to emergency surgery or to eye surgery
patient with propofol allergy or remifentanil allergy
Patient who has had a anesthesia between the 7 days before the study
Patient with a pacemaker
Patient with a transplant heart
Patient with previous history of parkinson disease, of diabetes, of chonic ethylism,
Patient with cardiac or autonomic disease
Patient with alpha or beta bloquant treatment
Patient with anti arythmic treatment
Patient allergic to soy or to peanut
Hypersensitivity to fentanyl derivatives or to one or mors Ultiva and Propofol excipient

Study & Design

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