Testing cotton to reduce discomfort from vibration anesthetic devices
Improving Patient Comfort of Vibratory Anesthetic Devices With a Cotton Dampener
NA · University Hospitals Cleveland Medical Center · NCT06916468
This study tests whether using cotton to soften the vibrations from anesthetic devices makes dermatology patients feel more comfortable during their procedures.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University Hospitals Cleveland Medical Center (other) |
| Locations | 1 site (Cleveland, Ohio) |
| Trial ID | NCT06916468 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of using cotton as a dampener for vibratory anesthetic devices (VADs) in dermatologic patients. It compares patient preferences for VADs with and without cotton across various anatomical sites and examines factors like chronic pain or neuropathy that may affect these preferences. The goal is to gather preliminary data that could lead to improvements in VAD usage, enhancing patient comfort during dermatologic procedures.
Who should consider this trial
Good fit: Ideal candidates are dermatologic patients aged 18 and older who can provide informed consent and complete the study session.
Not a fit: Patients with broken skin or known peripheral neuropathy at the site of vibration, as well as those with allergies to nitrile gloves or cotton, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve patient comfort during dermatologic procedures by optimizing the use of vibratory anesthetic devices.
How similar studies have performed: While there is limited information on similar studies, the approach of using dampeners to enhance comfort in anesthetic procedures is a novel concept that has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Age range: from 18+ 2. Dermatologic patients at Westlake Clinic 3. Consent: Must provide informed consent to participate in the study. 4. Availability: Able to complete the entire study session, which includes testing all sites in a single session Exclusion Criteria: 1. Broken skin or known peripheral neuropathy on anatomical site of vibration. 2. Allergies: Known allergy or sensitivity to nitrile gloves or cotton
Where this trial is running
Cleveland, Ohio
- University Hospitals — Cleveland, Ohio, United States (RECRUITING)
Study contacts
- Principal investigator: Bryan Carroll, MD — University Hospitals Cleveland Medical Center
- Study coordinator: Kymberlyn Warner
- Email: kymberlyn.warner@uhhospitals.org
- Phone: 216-844-7546
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Patient Care