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Perioperative Analgesie in der Gefäßchirurgie

Conditions
peripheral vascular disease, inclusion criteria: elective vascular surgery, age 30 to100years
male and female
exclusion Criteria: amaurosis, insufficient language skills, permanent opioid medication (morphin oral equivalent 80mg per day), permanent medication of tricyclic antidepressivs, history of adverse events to opioid medication
Registration Number
EUCTR2006-001951-36-AT
Lead Sponsor
Medical University of Vienna
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

see mentioned above
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) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

see mentioned above

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: comparison of quality in analgesic medication ( efficacy and adverse effects);Secondary Objective: differences regarding adverse effects;Primary end point(s): observation is finished on the third postoperative day; session planned four weeks after discharge to examine the developement of neuropathic pain
Secondary Outcome Measures
NameTimeMethod
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