Actively Recruiting

Phase 3
Age: 18Years +
All Genders
NCT07336368

Topical Cryotherapy and Keloid/Hypertrophic Scars

Led by Sonal Choudhary · Updated on 2026-05-06

30

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to determine whether the application of brief topical cryotherapy immediately before intralesional corticosteroid injections can reduce pain and injection resistance during routine treatment of keloid and hypertrophic scars in adult patients. The main questions it aims to answer are: Does topical cryotherapy applied before intralesional triamcinolone injection impact pain perceptions for participants with keloids or hypertrophic scars? Does topical cryotherapy affect provider-assessed injection resistance compared with standard injection alone? Researchers will split the keloid/hypertrophic scar into two halves. One half will be treated with cryotherapy followed by steroid injection, while the other half will be treated with steroid injection alone to evaluate differences in pain perception and injection resistance. Participants will rate pain after each injection using a 10-point numeric pain scale. Clinicians will rate the resistance after each injection using a 10-point numeric scale.

CONDITIONS

Official Title

Topical Cryotherapy and Keloid/Hypertrophic Scars

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults (18 years or older) with keloids or hypertrophic scars already scheduled for intralesional triamcinolone treatment
  • At least one keloid or hypertrophic scar with two comparable regions of 2 cm or more suitable for split-treatment
  • Able to provide informed consent and complete pain assessments in English
Not Eligible

You will not qualify if you...

  • Keloid or hypertrophic scar located on the face, except earlobes, excluded for cosmetic reasons
  • Prior treatment to the study-selected keloid or hypertrophic scar based on self-report
  • Inability to complete study assessments due to cognitive or language barriers

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

University of Pittsburgh

Pittsburgh, Pennsylvania, United States, 15213-3427

Actively Recruiting

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Research Team

S

Sonal Choudhary, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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