Münster, North Rhine-Westphalia, 48155, Germany
NCT Number: NCT00885937
Comparative Safety Study of New Sinecort Formulation Versus Positive Control
The study is focused to prove a favorable safety profile of the new formulation.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Age of at least 18 years
- Skin type I, II, or III according to Fitzpatrick
- Subjects of childbearing potential must use an acceptable method of contraception. Hormonal or oral contraceptive drugs, intra-uterine devices (IUD) and abstinence are considered acceptable methods of contraception.
Exclusion criteria
- Clinical history suggestive of intolerance, allergies or idiosyncrasies to one of the products or the ingredients of the products including the patch.
- Known skin allergies.
- Dermatologic diseases that might interfere with the evaluation of test site reaction.
- Other(s), considered as important by the investigator (e.g. multiple birth marks in the test area, important hair growth in the test area, pigmented or extremely suntanned skin impairing visual assessment, tattoos in the test area.
- Topical use of any cosmetic preparation on the test areas within 5 days prior to Day 1 (Start of Treatment) or during the trial
- Within 3 weeks prior to Day 1 and during the entire trial. Any systemic or topical medication likely to interfere with the trial purposes: e.g. immune-modulating therapy (e.g. corticosteroids, cytotoxics or immunosuppressants) and any dermatological medication (drug or medical device.
- Within 1 week prior to Day 1 and during the entire trial any medication with common effects on the perfusion of skin vessels (e.g. vasodilators or vasoconstrictors, ß-receptor blocking drugs, antihistamines) should not be used.
Treatment and study plan
Dexpanthenol (Sinecort, BAY81-2996)
Drug1 squeeze of Sinecort cream sufficient to cover the area of the application chamber, (=50 mikro liter)
Positive control, Na-laurylsulfat-solution
Drug50 mikro liter of 0.5 % Sodium-laurylsulfate-solution
Untreated skin under application chamber
DeviceApplication of treatment chamber as in arm 1 and arm 2 on untreated skin
Primary outcomes
-
Irritation rate
Time frame: After 21 applications
Secondary outcomes
-
Irritation potential
Time frame: After 21 applications
Sponsors and collaborators
Lead sponsor
Bayer
Industry
Registry information
Official study title
Single-blind, Randomized, Controlled, Single Center Trial to Evaluate the Skin Irritation Potential of a New Topical Formulation by Means of an Occlusive Patch Test in Healthy Subjects.
Important dates
- Study start
- 2009
- Primary completion
- 2009
- Study completion
- 2009
- First posted
- Apr 22, 2009
- Registry last updated
- Jun 23, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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