Official Title

Immunogenetic Profiling of Goeckerman Therapy in the Treatment of Psoriasis Vulgaris
  • Phase

    Phase 4
  • Study Type

    Interventional
  • Status

    Recruiting
  • Study Participants

    15
This study examines the effect of Goeckerman therapy (a combination of phototherapy and topical crude coal tar), crude coal tar alone, and phototherapy alone on the immunologic and genetic environment within psoriatic skin lesions.
This is a three-arm, open-label study to examine the effect of Goeckerman therapy. Goeckerman therapy is known for its high efficacy and favorable safety profile in the treatment of psoriasis. It consists of a combination of phototherapy and topical crude coal tar). This study will examine how Goeckerman therapy, crude coal tar alone, and phototherapy alone affect the mmunologic and genetic environment within psoriatic skin lesions. Fifteen subjects with moderate to severe psoriasis will be enrolled. Biopsy samples will be collected and undergo molecular profiling to further elucidate the mechanism of action by which Goeckerman treatment improves psoriatic skin lesions.
Study Started
Aug 01
2018
Primary Completion
Dec 31
2023
Anticipated
Study Completion
Dec 31
2023
Anticipated
Last Update
Apr 05
2023

Other Goeckerman Therapy

The Goeckerman regimen consists of exposure to narrowband ultraviolet B (NB-UVB) light phototherapy and application of crude coal tar to the skin 5 days per week. The treatment will occur the UCSF outpatient skin treatment center for approximately 4-5 hours, 5 days a week for 6 weeks (total of 30 sessions). The treatment is consistent with the standard of care Goeckerman treatment protocol at UCSF.

  • Other names: Combination Treatment with Phototherapy and Crude Coal Tar, Goeckerman Regimen

Drug Crude Coal Tar Only

A topical medication consisting of crude coal tar will be applied to the psoriatic skin under plastic wrap occlusion for approximately up to 4-5 hours, 5 days a week for 6 weeks (total of 30 sessions), at the outpatient skin treatment center at UCSF.

  • Other names: Coal tar

Device Phototherapy Only

Light treatment with narrowband ultraviolet B (NB-UVB) phototherapy three days per week for 12 weeks at the UCSF Phototherapy Center per the standard UCSF phototherapy protocol, in which starting dose is based on the subject's Fitzpatrick skin type and gradually increased as tolerated. Each phototherapy treatment will last approximately from under 1 minute to less than 15 minutes.

  • Other names: Ultraviolet B, Narrowband ultraviolet B, NB-UVB, UVB phototherapy, Phototherapy, Light treatment

Goeckerman Therapy Active Comparator

Patients with psoriasis who will receive Goeckerman therapy 5 days per week for 6 weeks.

Phototherapy Only Active Comparator

Patients with psoriasis who will receive narrowband ultraviolet B (NB-UVB) phototherapy 3 days per week for 12 weeks.

Crude Coal Tar Only Active Comparator

Patients with psoriasis who will receive skin treatment with crude coal tar only 5 days per week for 6 weeks.

Criteria

Inclusion criteria

Male or female ≥ 18 years of age at enrollment.
Documentation of predominately moderate to severe plaque psoriasis for at least 6 months prior to enrollment.
Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.
Subject is considered a candidate for phototherapy or systemic therapy
Body Surface Area (BSA) ≥ 5%.
Physical exam within clinically acceptable limits.

Exclusion criteria

Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
Subject has predominantly non-plaque form of psoriasis.
Subject has drug-induced psoriasis.
Subject with current, or a history of, severe psoriatic arthritis well controlled on current therapy.
Patient has absolute or relative contraindication to phototherapy, including photosensitizing disorders.
Evidence of abnormality of any immune cell population from a drug-induced or genetic cause.
Known HIV positive status.
Known allergy to lidocaine, other local anesthetics, or any component of local anesthetic agents.
No Results Posted