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Perioperative Analgesie in der Gefäßchirurgie

Perioperative Analgesie in der Gefäßchirurgie

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2006-001951-36-AT
Enrollment
Unknown
Registered
2006-04-12
Start date
2006-05-15
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

peripheral vascular disease, inclusion criteria: elective vascular surgery, age 30 to100years

Interventions

Trade Name: Oxycontin Product Name: Oxycodone Pharmaceutical Form: Film-coated tablet Pharmaceutical form of the placebo: Film-coated tablet Route of administration of the placebo: Oral use Trade Nam

Sponsors

Medical University of Vienna
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

Exclusion criteria: see mentioned above

Design outcomes

Primary

MeasureTime frame
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—

Countries

Austria

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026