Efficacy and Safety of HA35 Gel for Ultra-Rapid Skin Pruritus Relief
NCT: NCT07580911 · NOT_YET_RECRUITING
Brief Summary
This is a prospective, single-arm, open-label, pilot clinical study to evaluate the efficacy and safety of topical 10% high-concentration 35 kDa hyaluronan (HA35) gel for ultra-rapid relief of moderate-to-severe skin pruritus from diverse etiologies (eczema, neurodermatitis, insect bites, urticaria, postoperative wound itch). Eligible participants will receive a single topical application of HA35 gel. The primary objective is to assess pruritus relief at 10 seconds, 45 minutes, 8 hours, 12 hours, and 24 hours post-application. Safety and local skin tolerability will be evaluated throughout the observation period. This is a minimal-risk, non-pharmacological, non-invasive intervention.
Frequently Asked Questions
What is Efficacy and Safety of HA35 Gel for Ultra-Rapid Skin Pruritus Relief?
Efficacy and Safety of HA35 Gel for Ultra-Rapid Skin Pruritus Relief is a clinical trial registered under NCT07580911. Current status: NOT_YET_RECRUITING.
What is the status of NCT07580911?
The current status of NCT07580911 (Efficacy and Safety of HA35 Gel for Ultra-Rapid Skin Pruritus Relief) is: NOT_YET_RECRUITING.
When did Efficacy and Safety of HA35 Gel for Ultra-Rapid Skin Pruritus Relief start?
Efficacy and Safety of HA35 Gel for Ultra-Rapid Skin Pruritus Relief started on 2026-06-20.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.