MedTrace Logo

Serum Concentration of Lidocaine After Local Injection During Mohs Micrographic Surgery

NCT00793169 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 19

Last updated 2021-12-06

Study results available
· View outcomes & findings →

Summary

The primary objective of this study is to (1) determine whether local injection of lidocaine used during Mohs surgery will elevate serum lidocaine concentrations to a level that could cause systemic symptoms and (2) determine whether sustained high levels of serum lidocaine occur after intralesional anesthesia on the face and neck. This study is a cross-sectional study of 10 subjects with basal cell carcinoma or squamous cell carcinoma of the face or neck requiring Mohs micrographic surgery. The study will consist of a brief questionnaire and blood draws during their Moh's surgical procedure.

Conditions

Interventions

PROCEDURE

Blood Draw

Serum levels were measured

Sponsors & Collaborators

Principal Investigators

  • Murad Alam, MD · Northwestern University

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2008-07-31
Completion
2008-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases
Companies

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 NCT00793169 on ClinicalTrials.gov