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clinical demonstration research of

clinical demonstration research of

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002447
Enrollment
Unknown
Registered
2012-08-16
Start date
2012-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

psoriasis vulgaris

Interventions

A:PSORI-CMO1 decoction plus Calcipotriol Betamethasone Ointment
B:Placebo decoction plus Betamethasone Ointment

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Male and female aged 18 to 70 years old; 2. Patients with a PASI index more than 7 and less than or equal to 20, and BSA less than 30%; 3. signed written informed consent.

Exclusion criteria

Exclusion criteria: 1. Other types of psoriasis; 2. Pregnant or lactating women and menorrhagia women and women who plan to pregnant in one year; 3. Thestandard score of SAS more than 50points and the one of SDS more than 53points, or associated with mental illness; 4. Associatedwith cardiovascular, respiratory, digestive, renal and hematopoietic system ofprimary and serious diseases, or tumors, or serious infection, or water, electrolyte, acid-base balance disorders, especially calcium metabolism disorder; 5. Allergic to the drugs ingredients; 6. the patients who are participating in other clinical trial or have participated in other trials within the recent one month; 7. Patientswho were treated with glucocorticoids or externallyapplied agent such as retinoic acid or ultraviolet therapy over the pass 2 weeks, and treated with systematic therapy or biologics therapy over the pass 4 or 12 weeks respectively; 8. Need to receive systematic therapy.

Design outcomes

Primary

MeasureTime frame
relapse rate of Psoriasis vulgaris during the treatment period;PAS;

Secondary

MeasureTime frame
time interval until relapse;onset time;the dosage of external use for western medicine;VAS;DLQ;

Countries

China

Contacts

Public ContactLu Chuanjian
luchuanjian888@vip.sina.com+86 20 81887233-31223

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 13, 2026