Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Clinical Trial

Efficacy and Safety of HA35 Gel for Ultra-Rapid Skin Pruritus Relief

NCT: NCT07580911 · NOT_YET_RECRUITING

NCT IDNCT07580911
StatusNOT_YET_RECRUITING
Start Date2026-06-20
Completion2026-08-20

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.