Keloid Scars

3

Review clinical trials related to Keloid Scars. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Topical Cryotherapy and Keloid/Hypertrophic Scars

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.

Participants needed: 30
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Sonal ChoudharyUpdated: Jun 12, 2026Locations: 1
Eligibility criteria

Adults (≥18 years) with keloids or hypertrophic scars already scheduled to recei... [+2]

Keloid or hypertrophic scar located on the face (except earlobes), excluded for... [+2]

Status: Recruiting

Evaluation of Clinical, Perceived and Instrumental Efficacy of a Scar Gel in Preventing Hypertrophic Scars

Evaluation of the safety and topical efficacy of a scar gel after 90 days of continuous use, comparing it to a benchmark for preventing hypertrophic scars and improving appearance, hydration and pigmentation.

Participants needed: 80
Trial details
Phase: Phase 1, Phase 2Age: 18-70Biological sex: AllType: InterventionalSponsor: Herbarium Laboratorio Botanico LtdaUpdated: Sep 11, 2025Locations: 2
Eligibility criteria

Participants of both sexes aged between 18 and 70 years; [+5]

Pregnancy or risk of pregnancy; [+8]

Status: Not yet recruiting

Comparison of Intralesional Triamcinolone Versus Verapamil for Keloid Treatment

This study aims to compare the efficacy of intralesional triamcinolone and verapamil in patients presenting with keloid at our local setting. The results will guide us towards better management of keloids by choosing the more appropriate treatment. Adequate treatment will reduce significant emotional and physical distress in patients. We hypothesized that mean reduction in Vancouver Scar Score is higher in triamcinolone acetonide group compared to verapamil after three months of treatment.

Participants needed: 60
Trial details
Phase: Phase 4Age: 10-50Biological sex: AllType: InterventionalSponsor: Nishtar Medical UniversityUpdated: Apr 1, 2025Locations: 1
Eligibility criteria

size of keloid1-5 cm, [+3]

Pregnant or lactating women, [+3]