Evaluation of Cicaplast in Subjects With Skin Irritation

Completed

Conditions studied: Skin Diseases

In brief

The aim of this open, before/after, multicentric study is to assess the effect and tolerance of Cicaplast Baume B5 in patients having a skin irritation (irritative and cracked dermatitis, dry eczematids, rubbing irritation, ...) under dermatological control. Patients are asked to apply the product at least twice a day until complete recovery (maximum 21 days).

Key facts

Study ID

NCT05767333

Run by

Cosmetique Active International

People needed

109

Starts

2021-10-11

Expected to finish

2022-06-06

Last updated by the study team

2023-03-14

Who can join

Age: 3 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• subjects presenting the following skin irritations (at least 3 to 5 per irritation): irritative and cracked dermatitis, dry eczematids/dry patches, rubbing irritation in specific location (ex: thumb frictions, lichenifications), ...
• localization of irritation lesions: face, limbs, trunk, feet, fold, hands, ...
• subjects having a feeling of discomfort at the site of the lesion.

You may not qualify if…

• cutaneous pathology on the studied zone (other than the required irritations)
• use of topical or systemic treatment during the previous weeks liable to interfere with the assessment of the cutaneous acceptability of the study product (according to the investigator's appreciation);
• subject with healing disorder (keloid, hypertrophic)
• subject with Type 1 diabetic
• subject under chemotherapy and radiotherapy
• subject with a skin disease on evaluation site: psoriasis and atopic dermatitis active lesions and hand dermatitis

Where it is running

• EUROFINS CRL, Inc. — Piscataway, New Jersey, United States
• EUROFINS CONSUMER PRODUCT TESTING Co. Ltd — Guangzhou, China
• Insight Research — Quatre Bornes, Mauritius
• EUROFINS DERMSCAN POLAND Sp. — Gdansk, Poland

Full record on ClinicalTrials.gov

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