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Control of therapy of acne papulopustulosa by visible light with waterfiltered infrared and / or Adapalen (Differin Gel)

Conditions
Acne papulopustulos
Registration Number
EUCTR2005-004640-31-DE
Lead Sponsor
Technische Universität Dresden
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Age >= 14 years
Mild to moderate acne papulopustulosa according to Burton Scale Stage 3 to 4
At least 5 inflammatory and 5 non-inflammatory lesions in the face
Are the trial subjects under 18? yes
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Pregnant and nursin women
Antiandrogen therapy
Therapy with antibiotics within the last 4 weeks
Therapy with retinoids within the last 6 months.
Natural or artificial UV-therapy within the last 4 weeks
Severe acne papulopustulosa according to Burton Scale 5 or 6
Severe systemic condition
Alcohol or drug abuse
Noncompliant patients
Use of other acne therapeutics 2 weeks before and during the study
Secondyry acne (for example chlor and steroid acne)

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: Control of the effectiveness of visible light in combination with infrared light compared to Adapalen (Differin Gel);Secondary Objective: ;Primary end point(s): Reduction of inflammatory and non-inflammatory lewsions within 8 weeks after start of therapy.
Secondary Outcome Measures
NameTimeMethod
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