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Clinical Trials/NCT00528463
NCT00528463CompletedPhase 4

a Prospective Case Series of Pre-emptive Pre-amputation Sciatic Nerve Block to Prevent Lower Limb Phantom Pain

Université de Sherbrooke1 site in 1 country17 target enrollmentStarted: January 1, 2005Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Phase 4
Status
Completed
Enrollment
17
Locations
1
Primary Endpoint
incidence of lower limb phantom pain

Study Overview

Brief Summary

Phantom limb pain is a complication of amputation. Although pre-empitve epidural analgesia was once thought to prevent such a com plication, recent studies did not demonstrate this. Peripheral blocks are more powerful then epidurals, and can even influence somatotropic representation in the brain. This a prospective case series in which the investigators hope to show a decrease, against historical control, of the incidence of post-operative amputation lower limb phantom pain. The investigators established the block at least 24 hours pre-operative and continue it for at least 2 days. Patient are followed daily for the 1st 3 days and then up to 3 month for the incidence of phantom limb pain. The investigators hope to recruit 30 patients.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patient scheduled for lower limb amputation

Exclusion Criteria

  • •Inability to consent
  • •Contraindication to peripheral nerve block
  • •Inability to perform the block
  • •Inadequate time frame (less than 24 hours prior to surgery)

Arms & Interventions

sciatic block

Experimental

One arm, all patient studied received a block

Intervention: sciatic nerve block (Procedure)

Outcomes

Primary Outcomes

incidence of lower limb phantom pain

Time Frame: 3 month post amputation

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (1)

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