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RECRUITING
NCT07106957
NA

Efficacy and Safety Evaluation of CICAPLAST BAUME B5+ on Rosacea Accompanied by Sensitive Skin

Sponsor: Beijing Sino-German Union Cosmetic Institute Co., Ltd.

View on ClinicalTrials.gov

Summary

In total, 72 eligible research participants were recruited in this 56-day study. The participants were divided into two groups-namely the Experimental Group and the Control Group-according to stratified randomization, with 36 participants in each group. Finally, 30 participants in each group were expected to complete the study. In this study, for patients with rosacea accompanied by sensitive skin, differences in repairing effects and other improvements were evaluated after they used LA ROCHE-POSAY CICAPLAST BAUME B5+ and a standard cream for 28 days, as well as differences between the two groups after both groups used LA ROCHE-POSAY CICAPLAST BAUME B5+ for an additional 28 days-via objective instrumental measurements and subjective assessments. Additionally, the safety of the investigational product was evaluated among these individuals.

Official title: A Single-center, Randomized, Double-blind, Controlled Study Lasting for 56 Days to Evaluate the Safety and Efficacy of LA ROCHE-POSAY CICAPLAST BAUME B5+ in Individuals With Rosacea Accompanied by Sensitive Skin

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

72

Start Date

2025-06-10

Completion Date

2025-08-10

Last Updated

2025-08-06

Healthy Volunteers

No

Interventions

OTHER

CICAPLAST BAUME B5+

Twice a day (morning and evening) on face

OTHER

Standard cream

Twice a day (morning and evening) on face

Locations (1)

Beijing Sino-German Union Cosmetic Institute Co., Ltd.

Beijing, China