Prospective randomised controlled study on tumescent local anesthesia for Mohs Micrographic Surgery ( MMS) compared to conventional anesteshia with lidocaine/ epinephrine 1 %

Completed

• Conditions: Painsensation; 10040900

• Registration Number: NL-OMON34466
• Lead Sponsor: Catharina-ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 18

Inclusion Criteria

Patients with a basal cell carcinoma on the scalp, the nose, or the forehead, wich will be treated with Mohs micrographic surgery.

Exclusion Criteria

Allergy for lidocaine/epinephrine 1% or substances in the tumescent.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Registration of the pain perception during anesthesia.<br /><br>Registration of the pain during the operation .<br /><br>Registration of the pain postoperative . </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The duration of the anesthetic effects.<br /><br>The vasoconstrictive effects of the TLA.</p><br>