drugset / Trial / NCT06108193

Toxicity and Efficacy Evaluation of Topical Minoxidil in Acne Vulgaris

NCT06108193

Phase 1/2 Unknown 26 enrolled Chang Gung Memorial Hospital
NaSingle-groupOpen-labelTreatment

Summary

Patients with acne vulgaris (AV) appeared to be a chronic inflammation with a wide range in teenagers and adult. The protocol design is as follows. The subjects enrolled through inclusion and exclusion criteria will undergo the blood and urine biochemical tests for baseline record. The photos from the subjects will be recorded per day, and the blood and urine biochemical tests will be recorded per week. Objectives: primary: to test the toxicity of topical minoxidil in treatment of acne vulgaris; second: to evaluate the response and disease control rate in this pilot study. Measurement: Time to resolution of individual acne lesions (14 days) Monitor of treatment efficacy: number of inflammatory acne lesions counting, time to resolution of individual acne lesion, and degree of acne severity measurement.

Timeline

Start
2023-07-11
Primary completion
2023-12-31
Completion
2023-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Minoxidil Small molecule 2 % Topical
Subject Minoxidil Small molecule 5 % Topical

Indications