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Clinical evaluation of acupuncture with enhanced efficacy and reduced toxicity as an adjuvant to acitretin in the treatment of moderate to severe psoriasis vulgaris and its mechanism of action based on "treating the skin from the intestine"

Clinical evaluation of acupuncture with enhanced efficacy and reduced toxicity as an adjuvant to acitretin in the treatment of moderate to severe psoriasis vulgaris and its mechanism of action based on "treating the skin from the intestine"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108030
Enrollment
Unknown
Registered
2025-08-22
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Psoriasis

Interventions

Experimental Group (Acitretin + Acupuncture Group):Take acitretin and apply topical moisturizing to the skin. The dosage of acitretin is 30mg/ day. After the symptoms are controlled, reduce the dosage
Control group (Acitretin + sham acupuncture group):On the basis of systemic administration of acitretin and topical skin moisturizing, A sham acupuncture therapy was adopted.

Sponsors

Chengdu Pidu District Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18–70 years. 2.Diagnosed with psoriasis according to the clinical diagnostic criteria in Chinese Guidelines for the Diagnosis and Treatment of Psoriasis, with a course of plaque psoriasis = 6 months. 3.Baseline PASI score >= 10. 4.Signed informed consent form. 5.Dermatology Life Quality Index (DLQI) score > 10. 6.Previous ineffectiveness to topical medications.

Exclusion criteria

Exclusion criteria: 1.Severe infections. 2.Severe liver disease or clinical test results showing alanine transaminase (ALT)/aspartate transaminase (AST)/creatinine levels exceeding 1.5 times the upper limit of normal. 3.Alcoholic liver disease or other chronic liver diseases. 4.Renal failure. 5.Men and women planning to conceive within 3 months, pregnant women, and lactating women. 6.Patients with alcoholism. 7.Myelosuppression/hematological abnormalities (such as hypoplasia, leukopenia, thrombocytopenia, or severe anemia). 8.Patients with primary or secondary immunodeficiency. 9.Acute peptic ulcer. 10.Severe pulmonary insufficiency. 11.Patients allergic to acitretin or its related components. 12.Patients who have received systemic treatment within the past month. 13.Patients who have received biologic therapy within the past two months.

Design outcomes

Primary

MeasureTime frame
PASI 50 response rate;Self-depression (PHQ-9) scale scores;

Secondary

MeasureTime frame
The number of days with ASI=50% within 16 weeks of follow-up);Self-rated anxiety (GAD-7) scale scores;PASI 75 response rate;Change in DLQI score(Dermatology Life Quality Index score change);Doctor/Patient overall evaluation (4-level Likert scale score);Duration of drug effectiveness(Days from discontinuation to recurrence);Improvement rate of lesion area;Assessment of adverse drug events;

Countries

China

Contacts

Public ContactPeng Chang 'en

Chengdu Pidu District Hospital of Traditional Chinese Medicine

mikepen@sina.com+86 136 0819 7129

Outcome results

None listed

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