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Perioperative protective effects of lidocaine - clinical study on the route and timing of administratio

Conditions
patients, scheduled for major elective colorectal surgery
MedDRA version: 14.0Level: LLTClassification code 10040668Term: Sigmoid hemicolectomySystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: PTClassification code 10009879Term: Colectomy totalSystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: PTClassification code 10059848Term: ProctocolectomySystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: LLTClassification code 10019460Term: HemicolectomySystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: LLTClassification code 10039153Term: Right hemicolectomySystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: LLTClassification code 10024107Term: Left hemicolectomySystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: PTClassification code 10063950Term: IleocolectomySystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: PTClassification code 10042609Term: SurgerySystem Organ Class: 10042613 - Surgical and medical procedures
MedDRA version: 14.0Level: PTClassification code 10061778Term: ColectomySystem Organ Class: 10042613 - Surgical and medical procedures
Registration Number
EUCTR2007-000259-33-DE
Lead Sponsor
Department of Anesthesiology and Intensive Care, University Hospital Münster
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

- elective colorectal surgery
- ASA I-III
- age of 18 up to 85 years
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 150
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 150

Exclusion Criteria

-history of anti-inflammatory therapy
-history of inflammatory bowel disease
-history of chronic pain treatment
-history of or suspicion of allergy against local anesthetics

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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