Effects of Combination Therapy With Camouflage in the Repigmentation of Vitiligo
Primary Purpose
Vitiligo
Status
Completed
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
CapulinTM
topical applications and NB-UVB
Sponsored by
About this trial
This is an interventional supportive care trial for Vitiligo
Eligibility Criteria
Inclusion Criteria:
- Subjects who signed Informed Consent Form;
- Male or female subjects 16 years of age or older;
- Clinically confirmed diagnosis of vitiligo;
- Existing 2 symmetrical or adjacent white patches with similar size or a single lesion area greater than 5 cm2
Exclusion Criteria:
- Tend to automatically repigment;
- Allergic history of any relevant ingredient in the camouflage;
- The combination of eczema, contact dermatitis, urticaria and other allergic diseases or other serious diseases which are not suitable for the treatment of skin diseases;
- Women of child-bearing potential who are pregnant, plan to become pregnant during study or are lactating;
- Any other condition that the investigator deems unsuitable for entering the study.
Sites / Locations
- Peking university people's hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
camouflage group
blank group
Arm Description
Topical applications and/or NB-UVB plus Capulin TM on-demand treatment period
Topical applications and/or NB-UVB on-demand treatment
Outcomes
Primary Outcome Measures
Repigmentation area of vitiligo
The primary endpoint was percentage of repigmentation, assessed using photographs taken at baseline and each follow up visit. The photographs were shown to three dermatologists (blinded observers) for independent assessment and a mean of these values was taken.
Secondary Outcome Measures
types of regimentation types
The types of repigmentation patterns were classified as perifollicular, marginal, diffuse and mixed configuration.
Transepidermal water loss
TEWL at baseline and 12-week's follow-up between 2 groups
Adverse events
allergic reactions, edema, erythema, pruritis
Full Information
NCT ID
NCT03973073
First Posted
June 2, 2019
Last Updated
July 4, 2020
Sponsor
Peking University People's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03973073
Brief Title
Effects of Combination Therapy With Camouflage in the Repigmentation of Vitiligo
Official Title
Evaluation of the Potential Interference of Camouflage on the Treatment of Vitiligo: an Observer-blinded Self-controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
August 1, 2019 (Actual)
Primary Completion Date
November 1, 2019 (Actual)
Study Completion Date
November 21, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University People's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Vitiligo is a common depigmented skin disorder characterized by the white patches of skin and mucous membrane. It can be cosmetically disfiguring and lead to serious psychological problems for patients with vitiligo. In view of the difficulty of vitiligo treatment, the combination therapy is the most recommended. Despite that, the process of repigmentation usually last for several months to several years. So it is of great value to explore therapeutic methods that can improve appearance, relieve patients' pain and improve their quality of life in the process of treatment. The use of camouflage can vastly improve quality of life, both the European and Japanese guidelines of vitiligo management recommend that once vitiligo is diagnosed, camouflage should be used. The first commercial camouflage agent in China is CapulinTM by 2004. The main component of it is dihydroxyacetone. The repigmented mechanism is to combine with the keratin and to form a special brown polymer, which makes leukoderma close to normal skin. While, it is unknown whether camouflage has an impact on the drug absorption, efficiency of phototherapy and thus influences the repigmentation of vitiligo. Thus, the investigators undergo a randomized open-label self-controlled study to estimate the effects of combination therapy between camouflage and topical application and/or NB-UVB in the repigmentation of vitiligo.
Detailed Description
Vitiligo is a common depigmented skin disorder characterized by the white patches of skin and mucous membrane. It can be cosmetically disfiguring and lead to serious psychological problems for patients with vitiligo, especially when the exposed skin are involved, such as face and extremities.
The pathogenesis of vitiligo is not clear yet. The most common methods of treatment include systemic corticosteroids, topical application (such as corticosteroids, calcineurin inhibitors), phototherapy, traditional medications and so on. In view of the difficulty of vitiligo treatment, the combination therapy between drugs and phototherapy is the most recommended. Despite that, the process of repigmentation usually last for several months to several years. So it is of great value to explore therapeutic methods that can improve appearance, relieve patients' pain and improve their quality of life in the process of treatment.
For patients seeking to mask their vitiligo, camouflage options have historically been limited and been designated as a cosmetic, rather than a medical concern. As research has indicated that proper concealment of vitiligo lesions can vastly improve quality of life, we believe it is essential that dermatologists become aware of all the options available to their patients and that discussions of camouflage options be broached from the first visit. Until now, both the European and Japanese guidelines of vitiligo management recommend that once vitiligo is diagnosed, camouflage should be used.
The first commercial camouflage agent in China is CapulinTM by 2004. The main component of CapulinTM is dihydroxyacetone, and it also contains natural plant extracts, moisturizers, emollients and natural pigments. The repigmented mechanism is to combine with the keratin and to form a special brown polymer, which makes leukoderma close to normal skin.
Although the guidelines of home and abroad consider camouflage as the fundamental treatment of vitiligo, it is unknown whether camouflage has an impact on the drug absorption, efficiency of phototherapy and thus influences the repigmentation of vitiligo.
Thus, the investigators undergo a randomized observer-blinded self-controlled study to estimate the effects of combination therapy between camouflage and topical application and/or NB-UVB in the repigmentation of vitiligo.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitiligo
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
camouflage group
Arm Type
Experimental
Arm Description
Topical applications and/or NB-UVB plus Capulin TM on-demand treatment period
Arm Title
blank group
Arm Type
Other
Arm Description
Topical applications and/or NB-UVB on-demand treatment
Intervention Type
Combination Product
Intervention Name(s)
CapulinTM
Intervention Description
camouflage
Intervention Type
Other
Intervention Name(s)
topical applications and NB-UVB
Intervention Description
combination therapy of vitiligo
Primary Outcome Measure Information:
Title
Repigmentation area of vitiligo
Description
The primary endpoint was percentage of repigmentation, assessed using photographs taken at baseline and each follow up visit. The photographs were shown to three dermatologists (blinded observers) for independent assessment and a mean of these values was taken.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
types of regimentation types
Description
The types of repigmentation patterns were classified as perifollicular, marginal, diffuse and mixed configuration.
Time Frame
12 weeks
Title
Transepidermal water loss
Description
TEWL at baseline and 12-week's follow-up between 2 groups
Time Frame
12 weeks
Title
Adverse events
Description
allergic reactions, edema, erythema, pruritis
Time Frame
12 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Subjects who signed Informed Consent Form;
Male or female subjects 16 years of age or older;
Clinically confirmed diagnosis of vitiligo;
Existing 2 symmetrical or adjacent white patches with similar size or a single lesion area greater than 5 cm2
Exclusion Criteria:
Tend to automatically repigment;
Allergic history of any relevant ingredient in the camouflage;
The combination of eczema, contact dermatitis, urticaria and other allergic diseases or other serious diseases which are not suitable for the treatment of skin diseases;
Women of child-bearing potential who are pregnant, plan to become pregnant during study or are lactating;
Any other condition that the investigator deems unsuitable for entering the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juan Du, Doctor
Organizational Affiliation
Peking University People's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking university people's hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100044
Country
China
12. IPD Sharing Statement
Plan to Share IPD
No
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Effects of Combination Therapy With Camouflage in the Repigmentation of Vitiligo
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