ACTRN12615000782538
Completed
未知
A randomised, double blind, placebo controlled comparative trial of Ceramide Cream and Ceramide Cleanser in the management of moderate eczema in adults
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Ego Pharmaceuticals Pty Ltd
- Enrollment
- 100
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Male or females over 18 years of age.
- •2\. A confirmed diagnosis of eczema according to the criteria of Hanifin \& Rajka for at least one year, with moderate severity (score of 10\-20\) as evaluated with the EASI.
- •3\. Free of any dermatological or systemic disorder which could interfere with the results, at the discretion of the Investigator.
- •4\. Free of any acute or chronic disease that may interfere with or increase the risk of study participation.
- •5\. Completed a preliminary medical history form.
- •6\. Have read, understood and signed an informed consent document relating to the specific type of study they are subscribing.
- •7\. Able to cooperate with the Investigator and research staff, willing to have the test materials applied according to the protocol, and complete the full course of the study.
Exclusion Criteria
- •1\. Individuals under 18 years of age.
- •2\. History of allergies or adverse reactions to moisturisers or the components of the specific products being tested.
- •3\. Use of other moisturising products or other topical eczema therapies in the week prior to participation in this trial.
- •4\. Use of other moisturising products or other topical eczema therapies during the trial.
- •5\. Individuals taking any medication (topical or systemic) that may mask or interfere with the test results, i.e. calcineurin inhibitors, oral corticosteroids.
- •6\. A history of any acute or chronic disease that may interfere with or increase the risk of study participation.
- •7\. Excessive hair on the test sites.
- •8\. Individuals diagnosed with chronic skin allergies.
- •9\. Pregnant or nursing females.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not yet recruiting
Phase 4
Effectiveness of Herbal Oil in Osteoarthritis of KneeHealth Condition 1: M179- Osteoarthritis of knee, unspecifiedCTRI/2018/10/016235Gods Own Store LLP
Completed
Phase 1
ycopene supplementation in stable asthmaAsthmaRespiratory - AsthmaACTRN12606000286549Hunter New England Health Service139
Completed
Phase 2
A randomised placebo controlled clinical trial to study the therapeutic effectiveness of a Chinese herbal medicine formula used for the treatment of vascular dementia.Vascular dementia (VaD)Alternative and Complementary Medicine - Herbal remediesNeurological - DementiasACTRN12608000618358niversity of Western Sydney120
Recruiting
Not Applicable
Evaluation of the effect of transcutaneous electric nerve simulation (TENS) for the treatment of primary dysmenorrhea.Primary DysmenorrheaReproductive Health and Childbirth - Menstruation and menopauseACTRN12610000466044niversity of Pernambuco20
Completed
Phase 2
Chinese herbal medicine for Primary Dysmenorrhea.ACTRN12608000630314niversity of Western Sydney120