This Was a Clinical Study Investigating the Moisturization and Desquamation Effect of AmLactin® Rapid Relief Restoring Lotion + Ceramides on Dry Skin in Healthy Female Volunteers. AmLactin® Rapid Relief is an Over-the-counter Cosmetic

Sandoz

Status: Completed

Conditions: Dry Skin

Treatments: Other: AmLactin® Rapid Relief

Study type: Interventional

Funder types: Industry

Identifiers

NCT04085809

0123-02-01

Details and patient eligibility

About

The primary objective of this study was to investigate if AmLactin® Rapid Relief improves the skin through desquamation and moisturization via D-SQUAME analysis. AmLactin® Rapid Relief is an over-the-counter cosmetic.

Enrollment: 56 patients

Sex: Female

Ages: 50+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• healthy female (confirmed by medical history) with Fitzpatrick skin types I-VI
• dry, rough skin on the anterior shins (defined as Grade 3-4 on the dermatologist evaluation of the skin);

Exclusion criteria

• Had any visible skin disease at the assessment site which, in the opinion of the Investigator, would interfere with the evaluation of the test site

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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56 participants in 2 patient groups

Left Leg: AmLactin® Rapid Relief / Right Leg: No Treatment

Experimental group

Description:

AmLactin® Rapid Relief, BID application for 14 days on left leg and no treatment on right leg

Treatment:

Other: AmLactin® Rapid Relief

Left Leg: No Treatment / Right Leg: AmLactin® Rapid Relief

Experimental group

Description:

AmLactin® Rapid Relief, BID application for 14 days on right leg and no treatment on left leg

Treatment:

Other: AmLactin® Rapid Relief