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Clinical Trials/ACTRN12614001066673
ACTRN12614001066673
Recruiting
Phase 2

Effectiveness of the intercostobrachial nerve block compared to a placebo to reduce the upper limb tourniquet pain in patients undergoing forearm surgery

Department of Anaesthesia and Pain Medicine at Royal Perth Hospital0 sites20 target enrollmentOctober 3, 2014
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ConditionsTourniquet Pain during forearm surgeryAnaesthesiology - Anaesthetics

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Tourniquet Pain during forearm surgery
Sponsor
Department of Anaesthesia and Pain Medicine at Royal Perth Hospital
Enrollment
20
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 3, 2014
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Department of Anaesthesia and Pain Medicine at Royal Perth Hospital

Eligibility Criteria

Inclusion Criteria

  • •Forearm operation
  • •Suitable for axillary brachial plexus nerve block

Exclusion Criteria

  • •Age less than 18
  • •Weight less than 50 kg
  • •Unable to give informed consent themselves
  • •Intravenous drug users
  • •Chronic pain patients
  • •Those who are contraindicated to the nerve block
  • •Expected tourniquet inflating time is less than 45 minutes

Outcomes

Primary Outcomes

Not specified

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