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Comparison of Two Lidocaine Administration Techniques

NCT01330134 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 481

Last updated 2018-07-26

Study results available
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Summary

The objective of our study is to determine if technique of lidocaine administration can decrease pain perception.

Hypothesis: There will be a significant difference in pain perception between patients who are given lidocaine on the skin surface prior to subcutaneous injection and patients who are given only subcutaneous injection by standard approach.

Conditions

Interventions

DRUG

lidocaine

2ml 1% lidocaine placed onto surface of the skin immediately prior to 1% lidocaine subcutaneous injection

DRUG

lidocaine

1% lidocaine subcutaneous injection alone

Sponsors & Collaborators

  • University of Chicago

    lead OTHER

Principal Investigators

  • John P Kress, MD. · Univeristy of Chicago

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2015-04-30
Completion
2015-04-30

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01330134 on ClinicalTrials.gov