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Clinical Trials/EUCTR2006-005667-26-GB
EUCTR2006-005667-26-GBActive, not recruitingPhase 1

A randomised, placebo controlled trial of levobupivacaine or the combination of levobupivacaine and clonidine when administered as a sciatic perineural infusion for the prevention of phantom limb pain and cardiac morbidity after lower limb amputation - Incidence of phantom limb pain after lower limb amputation

inewells Hospital0 sites300 target enrollmentStarted: April 17, 2007Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Phase 1
Status
Active, not recruiting
Sponsor
Enrollment
300

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Inclusion Criteria

  • All patients presenting for elective lower limb amputation will be approached for recruitement to this 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) yes
  • F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • Patients excluded from the study will be those with signs of cardiac failure (3rd heart sound, lung crepitations), hypovolaemia, respiratory failure, presence of seizures, dementia, or encephalopathy, and patients with any terminal illness with a life expectancy < 3 months

Investigators

Sponsor
inewells Hospital

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