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Effect of treatment and mechanism with Chinese medicine PSORI-CM01, balneotherapy and coal tar on psoriasis vulgaris

Effect of treatment and mechanism with Chinese medicine PSORI-CM01, balneotherapy and coal tar on psoriasis vulgaris

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007615
Enrollment
Unknown
Registered
2015-09-01
Start date
2015-05-01
Completion date
Unknown
Last updated
2018-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

psoriasis

Interventions

Intervention group:PSORI-CMO1 granules+balneotherapy + coal tar
Control group:PSORI-CMO1 placebo granules+balneotherapy + coal tar

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients with psoriasis vulgaris; 2. Male or female patient between 18 to 65 years old; 3. PASI more than 10 and less than 30, and BSA more than 10 and less than 30; 4. Can read and understand by themselves; 5. Informed consent.

Exclusion criteria

Exclusion criteria: 1. Psoriatic lesions can only be seen on face, scalp, nails, balanus, mucus and palmarplantar areas; 2. Pregnant, lactating, or those who plan to become pregnant in a year; 3. SAS more than 50 or SDS more than 53, or with other psychiatric disorders; 4. With history of primary cardiovascular, respiratory, digestive, urinary, endocrinologic and hematologic diseases, which cannot be controlled through ordinary treatments. Those who with malignant diseases, infections, electrolyte imbalance, acid-base disturbance, acute infectious disease, wound, acute arthritis, malnutrition. Patients with clinical test results listed below: AST or ALT 3 times more than normal upper limit; Creatinine 1.5 times more than normal upper limit; Hemoglobin elevates 20g/L more than normal upper limit; Platelet count less than 75.0*10^9/L; White blood cell less than 3.0*10^9/L; Or any other abnormal laboratory test results, assessed by investigators, that are not suitable for this clinical study; 5. Allergic to any medicine or ingredients used in this study; 6. Participating other clinical trials or participated within 1 month; 7. Topical treatments with corticosteroids or Retinoic acid within 2 weeks; systemic therapy or phototherapy (UVB and PUVA) within 4 weeks; biological therapy within 12 weeks; 8. Psoriatic arthritis, and erythroderma tendency; 9. Patients need systemic treatment with western medicine.

Design outcomes

Secondary

MeasureTime frame
improvement rate of PASI;body surface area;Physician’s Global Assessment;visual analogue scale;self-administered psoriasis area and severity index;Dermatology Life Quality Index;Skindex16;

Primary

MeasureTime frame
Psoriasis Area and Severity Index score;Relapse rate in treatment period / follow-up period;

Countries

China

Contacts

Public ContactChuanjian Lu
luchuanjian888@vip.sina.com+86 13822250116

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026