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Clinical Trials/NCT02870595
NCT02870595
Completed
Not Applicable

The Use of Micro Vibratory Stimulation Technique to Control the Pain of Digit Block Anesthesia

Christus Spohn Memorial Medical Center0 sites25 target enrollmentJune 2014
ConditionsPain, Analgesia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Analgesia
Sponsor
Christus Spohn Memorial Medical Center
Enrollment
25
Primary Endpoint
Pain associated with injection of lidocaine
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The investigators hypothesize that patients who receive 1% lidocaine injections for digit blocks of the finger will experience less pain when the injection is accompanied by the use of a micro-vibratory stimulator (MVS) compared with patients who receive injections without the MVS.

Detailed Description

Research Question/Hypothesis The investigators hypothesize that patients who receive 1% lidocaine injections for digit blocks of the finger will experience less pain when the injection is accompanied by the use of a micro-vibratory stimulator (MVS) compared with patients who receive injections without the MVS. Objectives The primary objective of this study is to compare the pain rating scale from an exposure group (digit block injection with the aid MVS) and the control group (traditional injection).

Registry
clinicaltrials.gov
Start Date
June 2014
End Date
September 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Christus Spohn Memorial Medical Center
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy individuals between the ages of 18 and 65 who are willing and able to consent and who require the use of local anesthetic digit block to both sides of a finger for the treatment of wounds, injuries, infections, or laceration of the fingers.

Exclusion Criteria

  • Allergy to any type of local anesthetic.
  • Inability to Consent.
  • Inability to complete a numeric pain scale.
  • Clinical appearance or clinical evidence of intoxication.
  • Significant compromising conditions such as major trauma and severe respiratory distress.

Outcomes

Primary Outcomes

Pain associated with injection of lidocaine

Time Frame: 30 seconds

Subjects will rate pain of injection using a 0-10 VAS

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