Psoriasis、Indigo Naturalis、Chinese Medicine Medicated Bath
NCT ID: NCT04117919
Last Updated: 2019-10-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
PHASE2
30 participants
INTERVENTIONAL
2019-10-05
2020-03-03
Brief Summary
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This is a single site, randomized, single-blind, controlled pilot study of Jing- Fu-Yau-Yu-Bau as a complementary therapy to treat mild to moderate plaque- type psoriasis during an 8-week period. We estimate to enroll 30 subjects (treatment group(N=15); controlled group(N=15)). We plan to investigate the efficacy and safety of Jing-Fu-Yau-Yu-Bau in Chinese subjects with mild to moderate plaque-type psoriasis.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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chinese medicine medicated bath
we used the leaf of paper mulberry as chinese medicine medicated bath. Two packs per day ,and the period of treatment will be two month.
paper mulberry leaf
Topical steroids+paper mulberry leaf The botanical origin of paper mulberry leaf is Broussonetia papyrifera (L.) Vent.
Triamcinolone (Encort-A) 0.1%15g/Tube
only Topical steroids
control group
Topical steroids
Triamcinolone (Encort-A) 0.1%15g/Tube
only Topical steroids
Interventions
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paper mulberry leaf
Topical steroids+paper mulberry leaf The botanical origin of paper mulberry leaf is Broussonetia papyrifera (L.) Vent.
Triamcinolone (Encort-A) 0.1%15g/Tube
only Topical steroids
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* had a diagnosis of plaque-type psoriasis for ≥6 months,
* a Physician's Global Assessment (PGA) score of 2-3, \<20% total body surface area (BSA) involvement, and a target plaque of ≥4 cm2.
Exclusion Criteria
* rebound/flare of chronic psoriasis,
* history of psoriatic arthritis,
* current drug-induced psoriasis,
* pregnant/nursing/planning pregnancy (men and women),
* used biologics within 3 months or 5 times the half-life,
* received phototherapy/systemic treatment within 4 weeks,
* topicals within 2 weeks,
* any systemic immunosuppressants within 4 weeks, -lithium/antimalarial/intramuscular gold within 4 weeks,
* tested positive for HIV/hepatitis B/C,
* had a history of alcohol/drug abuse,
* clinically-significant laboratory abnormality,
* sensitivity to Chinese herbs ,or allergy to leaf of paper mulberry.
* had skin wound or skin infection
* had current signs/symptoms of severe, progressive, or uncontrolled medical conditions, or were participating concurrently in an investigational study.
20 Years
65 Years
ALL
No
Sponsors
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China Medical University Hospital
OTHER
Responsible Party
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Principal Investigators
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Hui-Man Cheng
Role: STUDY_CHAIR
China Medical University Hospital
Locations
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No. 91, Xueshi Rd., North Dist., Taichung City 404, Taiwan (R.O.C.)
Taichung, , Taiwan
Countries
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Central Contacts
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Facility Contacts
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Hui-Man Cheng
Role: primary
Other Identifiers
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CMUH107-REC2-182
Identifier Type: -
Identifier Source: org_study_id
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