RecruitingPhase 4NCT06694714

Split Face Study of the Duration of Local Anesthetics - Fourth Arm

Characterizing and Comparing the Duration of Local Anesthetic in Dermatologic Surgery - Fourth Arm


Sponsor

Weill Medical College of Cornell University

Enrollment

35 participants

Start Date

Jan 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a research study to compare how long injectable pain medications (anesthetics) commonly used in dermatologic surgery are effective for. The investigators will investigate the role of anesthetic volume on the duration of action at highly vascular sites.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Male or female ≥ 18 years of age
  • Normal skin sensation at both nasal ala assessed by pinprick
  • Ability to provide informed consent

Exclusion Criteria3

  • Previous adverse reaction to local anesthetic or any components of the local anesthetics being evaluated
  • Pregnant or breastfeeding volunteers (assessed by self-report)
  • Patients taking monoamineoxidase inhibitors (MAOI) or antidepressants of the triptyline or imipramine types

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUG0.5 ml lidocaine + epinephrine 1:100,000

0.5 ml lidocaine + epinephrine 1:100,000, buffered 1/10 with sodium bicarb

DRUG1.0 ml lidocaine + epinephrine 1:100,000

1.0 ml lidocaine + epinephrine 1:100,000, buffered 1/10 with sodium bicarb


Locations(1)

Weill Cornell Medicine

New York, New York, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06694714


Related Trials