Clinical Trials Directory

Trials / Completed

CompletedNCT03852563

A Study to Gain Information How Well Dexpanthenol Derma Cream Helps the Face Skin to Recover After Cosmetic Lasering

Evaluation of the Safety and Efficacy of the Product Bepantol® Cream After the Dermatological Procedure in the Face.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
33 (actual)
Sponsor
Bayer · Industry
Sex
Female
Age
30 Years – 60 Years
Healthy volunteers
Accepted

Summary

In this study, researchers want to learn more about the effect of dexpanthenol cream on skin recovery and reduction of skin rash after a dermatological procedure (ablative laser) on the face for treatment of fine wrinkles, scars and open pores in adult women. After the dermatological procedure, participants will return within 3 weeks for 4 visits to the study center to investigate the skin conditions such as redness, irritation, softness and possible side effects. In addition, study participants will be asked about their general acceptance of dexpanthenol cream.

Detailed description

The primary objective is to evaluate the efficacy of the test product to aid skin recovery and reduction of erythema after ablative lasering on the face. Secondary objectives comprise clinical efficacy with respect to skin hydration, softness, vitality, appearance etc. and skin recovery, consumer judgement of product performance and acceptability, and safety.

Conditions

Interventions

TypeNameDescription
DRUGBAY207543 (Bepanthol)Product is applied to one hemiface.
OTHERSemisolid vaselineProduct is applied to one hemiface.

Timeline

Start date
2019-03-18
Primary completion
2019-04-22
Completion
2019-04-22
First posted
2019-02-25
Last updated
2020-04-20

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT03852563. Inclusion in this directory is not an endorsement.