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Control of Therapy of Acne Papulopustulosa by Visible Light With Waterfiltered Infrared and / or Adapalen (Differin Gel)

T

Technische Universität Dresden

Status and phase

Unknown
Phase 4

Conditions

Acne Papulopustulosa

Treatments

Radiation: VIS and wIRA
Drug: Adapalen

Study type

Interventional

Funder types

Other

Identifiers

NCT00237978
TUD-Akne02-003

Details and patient eligibility

About

The aim of the study is to investigate the effectivity of visible light in combination with waterfiltered infrared in treating acne papulopustulosa. The reduction of inflammatory and non-inflammatory lesions within 8 weeks will be measured and compared with the standard treatment with Adapalene.

Enrollment

60 estimated patients

Sex

All

Ages

14+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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
  • Age >= 14 years

Exclusion criteria

  • pregnant and nursing 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
  • Secondary acne

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 3 patient groups

1
Active Comparator group
Description:
VIS and wIRA
Treatment:
Radiation: VIS and wIRA
2
Active Comparator group
Description:
VIS, wIRA and Adapalen
Treatment:
Drug: Adapalen
Radiation: VIS and wIRA
3
Active Comparator group
Description:
Adapalen
Treatment:
Drug: Adapalen

Trial contacts and locations

1

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Central trial contact

Roland Aschoff, MD

Data sourced from clinicaltrials.gov

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