plaque psoriasis
Conditions
Interventions
Group 1:1-2W: Halometasone Cream, qd, am
Benvimod Cream, qd, pm
3-4W: Benvimod Cream, bid, Monday to Friday
Halometasone Cream, bid, Saturday and Sunday
5-8W: Benvimod Cream, bid.
Group 2:1-2W: Halometasone Cream, qd, am
Calcipotriol Ointment, qd, pm
3-4W: Calcipotriol Ointment, bid, Monday to Friday
5-8W: Calcipotriol Ointment, bid.
Sponsors
The Third Affiliated Hospital of Guangxi Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Male and female patients with plaque psoriasis aged 18 to 65 years; 2. A clinical diagnosis of stable plaque psoriasis representing a maximum of 10% of their total body surface area (excluding the face, groin, scalp, and genital regions); 3. Have a baseline PGA of >=2; 4. Have a minimum of one plaque that is at least 2*2cm in size; 5. In good general health and free of any disease state or physical condition that might impair evaluation of plaque psoriasis; 6. WOCBP using and willing to continue to use adequate contraceptive precautions for the duration of the study; 7. Willing and able to comply with the protocol and attend all study visits, provide written informed consent prior to the initiation of any study-related procedures.
Exclusion criteria
Exclusion criteria: 1. Other concomitant serious illness or medical condition (e.g., human immunodeficiency virus, renal insufficiency, clinically significant abnormal laboratory values) that could put a patient at risk during the study; 2. ALT or AST representing liver function is two times larger than the upper limit of normal value, or serum creatinine representing renal function, is higher than the upper limit of normal value; 3. The current diagnosis of non-plague form psoriasis (such as erythema, guttate and joint psoriasis), and progression of psoriasis vulgaris,drug-induced psoriasis vulgaris; skin lesions reach more than 10% of total body surface; 4. Palmoplantar psoriasis; 5. Pregnancy, lactation or who plan to be pregnant; 6. Known or suspected hypersensitivity to any of the constituents of the investigational product; 7. Treatment with other investigational drug within three months of day 0 or current participation in another clinical trial; 8. Alcohol dependent patients; 9. The frequent use of herb, sedatives, hypnotics, stabilizer and other addictive drugs; 10. Any other skin diseases that might interfere with the clinical assessment of plaque psoriasis and/or put the patient at risk; 11. Systemic immunomodulatory therapy known to affect psoriasis and decreases immune cell populations (e.g., alefacept) within 36 weeks prior to the baseline visit; 12. Any phototherapy (including laser), photo-chemotherapy, or systemic psoriasis therapy (such as systemic corticosteroids, methotrexate, retinoids, or cyclosporine) within four weeks prior to the baseline visit; 13. Topical anti-psoriatic therapy (including topical retinoids and vitamin D analogs) on the areas to be treated within two weeks prior to the baseline visit; 14.The subjects may not the study because of other reasons, or whose researchers think are unsuitable for this study;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PASI;PGA;Adverse Events;recurrence free rate of psoriasis in six months; | — |
Countries
China
Contacts
Public ContactLi Jianmin
The Third Affiliated Hospital of Guangxi Medical University
Outcome results
None listed