Actively Recruiting

Phase Not Applicable
Age: 22Years - 70Years
All Genders
Healthy Volunteers
NCT05066113

Feasibility Study on Radiofrequency-Based Selective Electrothermolysis to Investigate Its Effects on Human Skin

Led by Johns Hopkins University · Updated on 2025-06-11

50

Participants Needed

1

Research Sites

572 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research is being done to assess the effect of radiofrequency (RF)-based treatment on skin and skin conditions.

CONDITIONS

Official Title

Feasibility Study on Radiofrequency-Based Selective Electrothermolysis to Investigate Its Effects on Human Skin

Who Can Participate

Age: 22Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy volunteers and hidradenitis suppurativa (HS) patients aged 22 to 70 years
  • Healthy enough to undergo multiple skin biopsies as determined by the investigator
  • Ability to provide informed consent
  • Willingness and ability to follow all study procedures and attend scheduled visits
  • Ability to understand and communicate with the investigator
  • For HS patients: localized mild to moderate disease in the axillae with no active infection as assessed by the investigator
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Recently treated for skin diseases affecting clinical evaluation
  • Known contraindications to selective electrothermolysis treatment
  • Immunocompromised status
  • Use of systemic steroids or immune modulators
  • Use of blood thinners or bleeding disorders
  • Any active or currently treated infections
  • Significant medical history or illness making biopsy unsafe
  • Noncompliance with study requirements
  • Pregnancy or nursing (with hCG testing before each treatment)
  • Allergy to anesthetics
  • History of keloids or hypertrophic scars in the past 10 years
  • Use of oral/topical antihistamines, analgesics, or medications impacting the study
  • Use of medications impairing wound healing in the past 12 months
  • Inability to undergo required motor strength and sensory testing for adverse event assessment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Johns Hopkins School of Medicine

Baltimore, Maryland, United States, 21287

Actively Recruiting

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Research Team

R

Ruizhi Wang

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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