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

Primary Purpose

Eczema

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Physiogel AI Lotion, Physiogel Lotion
Sponsored by
University Hospital Muenster
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Eczema focused on measuring dry skin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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).

Sites / Locations

  • Department of Dermatology

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

I

II

Arm Description

Physiogel AI Lotion

Physiogel Lotion twice daily

Outcomes

Primary Outcome Measures

Improvement of dry skin Improvement of burning, stinging and pruritus (if present) Improvement of quality of life
Improvement of burning, stinging and pruritus (if present)
Improvement of quality of life

Secondary Outcome Measures

Full Information

First Posted
April 14, 2008
Last Updated
July 6, 2010
Sponsor
University Hospital Muenster
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1. Study Identification

Unique Protocol Identification Number
NCT00663364
Brief Title
Care of the Dry Skin With Physiogel AI Lotion® (W0156)
Official Title
Klinische Untersuchung Zur Pflege Trockener Haut Mit Physiogel AI Lotion Und Physiogel Lotion
Study Type
Interventional

2. Study Status

Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
July 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital Muenster

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eczema
Keywords
dry skin

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
I
Arm Type
Active Comparator
Arm Description
Physiogel AI Lotion
Arm Title
II
Arm Type
Active Comparator
Arm Description
Physiogel Lotion twice daily
Intervention Type
Drug
Intervention Name(s)
Physiogel AI Lotion, Physiogel Lotion
Intervention Description
Physiogel AI Lotion and Physiogel Lotion is a cosmetic, applied twice daily to dry skin
Primary Outcome Measure Information:
Title
Improvement of dry skin Improvement of burning, stinging and pruritus (if present) Improvement of quality of life
Time Frame
two weeks
Title
Improvement of burning, stinging and pruritus (if present)
Time Frame
two weeks
Title
Improvement of quality of life
Time Frame
two weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients age: over 18 years Willing to apply skin care for 2 to 4 weeks, twice daily 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: Participation in any other research study during the previous 4 weeks. Previous participation in this study. Concurrent participation in any other research study involving an investigational product. Current need for the use of topical steroids. History of skin disease or allergy likely to interfere with the study or known sensitivity to the test product or its ingredients. Subjects considered unable or unlikely to fulfill diaries. Employees of (CRO) or Stiefel Laboratories, or an immediate family member (partner, offspring, parents, siblings or sibling's offspring) of an employee. History of cancer. Recent immunization (less than 10 days prior to the use of the test product).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sonja Ständer, MD
Organizational Affiliation
Department of Dermatology, University Hopsital Münster
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Dermatology
City
Münster
State/Province
NRW
ZIP/Postal Code
48149
Country
Germany

12. IPD Sharing Statement

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

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