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A pilot study for the effect of infliximab on endothelial function in patients with psoriasis

Not Applicable
Recruiting
Conditions
Psoriasis vulgaris, Psoriatic arthritis, Pustular psoriasis, Erythrodermic psoriasis
Registration Number
JPRN-UMIN000027208
Lead Sponsor
The University of Tokyo Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
25
Inclusion Criteria

Not provided

Exclusion Criteria

1. Patients who are treated with other biologics within 3 months 2. Patients treated with cyclosporine within 2 weeks 3. Patients with the past history of severe hypersensitivity or anaphylaxis against infliximab or drugs including murine proteins. 4. Patients with or suspected of having malignancy 5. Patients with serious infection, such as sepsis and positivity of Hepatitis B virus antigen 6. Patients with active or the past history of tuberculosis 7. Patients with active or the past history of demyelinating diseases 8. Patients with congestive heart failure 9. Patients with serious liver diseases (more than 300 IU of AST or ALT) 10. Patients with serious kidney diseases (serum creatinine >= 2.0mg/dl) 11. Patients under or suspected of pregnancy 12. Patients under breast feeding 13. Patients who are regarded to be inappropriate for this study by doctors

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The percentage improvement in reactive hyperemia index measured by EndoPAT at 4 hours after the third infusion compared with the baseline
Secondary Outcome Measures
NameTimeMethod
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