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NCT05295979CompletedPhase 2

Chinese Medicine for Patients With Psoriasis

Development of a Novel Chinese Medicine Formula for the Treatment of Psoriasis: A Randomized, Double-blinded, Placebo-controlled Trial

Source: ClinicalTrials.gov · Last updated 27 Jul 2026

Brief summary (registry, in English)

Psoriasis is an inflammatory skin disease with huge negative impact on the quality of life of the patients, and has an overall prevalence of 2% to 3% in the general population. Plaques psoriasis is the most common type of the disease and presents red, well demarcated, and silvery plaques mainly localized in the umbilical and lumbosacral area as well as in the elbows, knees, and scalp. Currently, pharmacological treatments such as retinoids, corticosteroids, vitamin D analogs and biologics remain the main options for most psoriasis patients. However, side effect and high cost barred many ordinary psoriasis patients. A Chinese medicine formula "Inflammatory skin disease formula (ISDF)" was prescribed by Prof. Lin for many years and observed to be effective in relieving atopic dermatitis and psoriasis patients' clinical manifestations. In this study, subjects with psoriasis will be randomized into treatment group of "ISDF" or placebo group for 12 weeks.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
60 (actual)
First submitted
24 Feb 2022
Start date
20 Mar 2023
Primary completion date
27 Mar 2026
Lead sponsor
Chinese University of Hong Kong
Diseases
Psoriasis
NCT number
NCT05295979

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 60
  • From 20 Mar 2023 to the primary completion date, 27 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Systemic therapy for psoriasis 6 months prior to baseline.
  • Use topical medications for psoriasis 14 days prior to baseline such as retinoids, corticosteroids, vitamin D analogues, tazarotene and tacrolimus.
  • Has taken any antibiotics, probiotics and prebiotics 30 days prior to baseline.
  • UV light therapy 30 days prior to baseline.

Other illness

  • Psoriatic arthritis with syndrome of spleen-kidney yang deficiency according to Chinese medicine theory.
  • History of allergy to Chinese herbs.
  • Any other condition that in the opinion of the investigators could compromise the study.

Lab values

  • Clinically significant laboratory abnormality in blood, liver or renal functions (≥1.5 times the upper limit of reference range).

Other

  • Pustular or generalized erythrodermic psoriasis.
  • Unwillingness to comply with study protocol.

Who the study is looking for

  • Mild to moderate chronic plaque psoriasis (PASI score 3 to 12).
  • Willingness to give informed consent.

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hong Kong Institute of Integrative Medicine
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.