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Care of the Dry Skin With Physiogel AI Lotion® (W0156)

Klinische Untersuchung Zur Pflege Trockener Haut Mit Physiogel AI Lotion Und Physiogel Lotion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00663364
Enrollment
100
Registered
2008-04-22
Start date
2008-04-30
Completion date
2009-11-30
Last updated
2010-07-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eczema

Keywords

dry skin

Brief summary

Dry skin is a physiological condition and is characterized in contrast to greasy skin by roughness, desquamation and lack of brightness of the skin surface. Subjectively, feelings of tension, burning and itching can occur. Dry skin needs special care due to its structural and functional characteristics.We monitor an application test the Dermatocosmetics Oilatum Physiogel AI Lotion and Physiogel Lotion. This is to be accomplished with patients having dry skin. The influence on the roughness of skin, desquamation, feeling of tingle, burning and itching should be documented. If sleep quality is disturbed by tingle or itch, this will be monitored, too.

Detailed description

The included patients use the lotion twice daily for a two-week period. If not sufficient it can be continued up to a four-weeks period. Additionally, the patient receives a documentation sheets to note several parameters. In a sensory assessment, product specific parameter such as spreadability, permeability, lubricating, smell of lotion and cosmetic acceptance during the treatment will be assessed (at the beginning, after 2 weeks, after 4 weeks, 2 weeks after stopping treatment). After four weeks the skin care measurement will be terminated and the patient can continue with a treatment of his choice. A monitoring of at least 50 patients per preparation is intended.

Interventions

DRUGPhysiogel AI Lotion, Physiogel Lotion

Physiogel AI Lotion and Physiogel Lotion is a cosmetic, applied twice daily to dry skin

Sponsors

University Hospital Muenster
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients age: over 18 years 2. Willing to apply skin care for 2 to 4 weeks, twice daily 3. Willing to fulfill questionnaires / home diaries: self-perception of roughness of the skin, desquamation of the skin, lack of skin brightness, feelings of tension and itching

Exclusion criteria

1. Participation in any other research study during the previous 4 weeks. 2. Previous participation in this study. 3. Concurrent participation in any other research study involving an investigational product. 4. Current need for the use of topical steroids. 5. History of skin disease or allergy likely to interfere with the study or known sensitivity to the test product or its ingredients. 6. Subjects considered unable or unlikely to fulfill diaries. 7. Employees of (CRO) or Stiefel Laboratories, or an immediate family member (partner, offspring, parents, siblings or sibling's offspring) of an employee. 8. History of cancer. 9. Recent immunization (less than 10 days prior to the use of the test product).

Design outcomes

Primary

MeasureTime frame
Improvement of dry skin Improvement of burning, stinging and pruritus (if present) Improvement of quality of lifetwo weeks
Improvement of burning, stinging and pruritus (if present)two weeks
Improvement of quality of lifetwo weeks

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026