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Clinical Trials/NCT02086292
NCT02086292
Completed
Not Applicable

The Influence of Lidocaine Volume on Discomfort During Administration of Local Anesthetic

Norwegian University of Science and Technology1 site in 1 country36 target enrollmentFebruary 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Needlestick Injuries
Sponsor
Norwegian University of Science and Technology
Enrollment
36
Locations
1
Primary Endpoint
pain
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The aim of the study is to find a simple method for pain reduction that can be used in clinical practice when administering digital nerve block with a single subcutaneous injection. It will be investigated whether a smaller volume of lidocaine can decrease pain during injection.

Detailed Description

Healthy volunteers will receive a single subcutaneous injection digital nerve block at the base of each ring finger. 2ml 1% lidocaine in one of the fingers, and 1 ml 2% lidocaine in the other. After each injection, the subject will be asked to evaluate the pain on a visual analog scale (0-100 mm). Additionally the sensibility will be tested with a Semmes-Weinstein monofilament, to evaluate if the different methods achieve desired anesthetic effect.

Registry
clinicaltrials.gov
Start Date
February 2014
End Date
June 2014
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age 18 - 65

Exclusion Criteria

  • regular use of analgesics
  • known hypersensitivity of local anaesthetic
  • renal-, heart- or liver disease
  • known peripheral neuropathy or diabetes mellitus
  • local infection on injection site
  • circulation disorders in upper extremities (e.g. Raynaud´s phenomenon)

Outcomes

Primary Outcomes

pain

Time Frame: 60 seconds

1. visual analog scale 0-100mm 2. questionnaire

Study Sites (1)

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