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NCT Number: NCT07724418

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

This study will compare how long local anesthesia lasts when it is injected into different layers of the skin on the forearm. The investigators hypothesize that the numbing effect will last for different amounts of time depending on whether the medication is injected just under the skin or into the skin itself.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

About this study

This study will compare the relative duration and efficacy of a commonly used local anesthetic (lidocaine with epinephrine) when administered into different layers of the skin on the ventral forearm within the same participant. Specifically, injections will be placed in the intradermal and subcutaneous tissue. A modification of a previously published noninvasive pinprick testing method will be used to assess the duration of local anesthesia. The investigators hypothesize that the duration of anesthesia will differ depending on the depth of injection, with intradermal and subcutaneous administration producing different durations of anesthetic effect.

This study record uses the same protocol document of a previous study under Clinical Trials record NCT06694714, but documents a fifth arm for which data will be analyzed separately from data in NCT06694714.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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

Treatment and study plan

Lidocaine HCl/Epinephrine

Drug

Injection of lidocaine solution for local anesthesia. Participants will receive lidocaine via either intradermal or subcutaneous administration at a volume of 0.5 mL or 1.0 mL.

Primary outcomes

  1. Duration of anesthesia

    Time frame: From injection until return of sharp sensation, up to 6 hours

    Time (in minutes) from onset of anesthesia (loss of sharp sensation at the injection site) to return of sharp sensation.

  2. Onset of anesthesia

    Time frame: Immediately following injection until loss of sharp sensation, up to 10 minutes

    Duration (in minutes) between anesthetic administration to loss of sensation to sharpness at injection site.

Study contacts

Contact information is provided by the study sponsor or research team.

Fengrui Zhan, BS

CONTACT

[email protected]

6073797248

Kira Minkis, MD, PhD

CONTACT

[email protected]

6469627948

Sponsors and collaborators

Lead sponsor

Weill Medical College of Cornell University

Other

Registry information

Official study title

Characterizing and Comparing the Duration of Local Anesthetic in Dermatologic Surgery

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jul 24, 2026
Registry last updated
Jul 24, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.