Clinical Trials Directory

Trials / Completed

CompletedNCT06916468

Efficacy of Cotton as a Dampener for Vibration Anesthetic Device

Improving Patient Comfort of Vibratory Anesthetic Devices With a Cotton Dampener

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
53 (actual)
Sponsor
University Hospitals Cleveland Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The study aims to determine the effectiveness of cotton as a dampener for vibratory anesthetic devices (VADs) for dermatologic patients. It will compare patient preferences for VAD use with and without cotton across different anatomical sites and identify factors, such as chronic pain or neuropathy status, that may influence these preferences. Finally, the study seeks to generate preliminary data to inform potential modifications to VAD use, optimizing patient comfort in dermatologic procedures

Conditions

Interventions

TypeNameDescription
DEVICEVAD with Cotton DampenerA standard pen-like Vibratory Anesthetic Device (VAD) with cotton will be applied across five anatomical sites (lateral nasal wall, sub-malar region of the cheek, ear helix, lateral neck, and dorsal side of the forearm) of participants. For each anatomical site, one side (either right or left) will receive vibration with cotton, and the opposite side will receive vibration without cotton in a randomized order.
DEVICEVibratory Anesthetic Device (VAD)A standard pen-like Vibratory Anesthetic Device (VAD) without cotton will be applied across five anatomical sites (lateral nasal wall, sub-malar region of the cheek, ear helix, lateral neck, and dorsal side of the forearm) of participants.

Timeline

Start date
2025-04-30
Primary completion
2025-05-14
Completion
2025-05-14
First posted
2025-04-08
Last updated
2025-11-04
Results posted
2025-11-04

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06916468. Inclusion in this directory is not an endorsement.