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Observation on the efficacy of cyclosporine in the treatment of acute generalized exanthematous pustulosis

Observation on the efficacy of cyclosporine in the treatment of acute generalized exanthematous pustulosis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081074
Enrollment
Unknown
Registered
2024-02-21
Start date
2024-02-23
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

Acute generalized exanthematous pustulosis

Interventions

Cyclosporine group:Oral cyclosporine (3mg/kg/d ,q12h,5day 1.5mg/kg/d,q12h,2day)
Hormone groupv:The method of intravenous infusion is to use 1mg/kg of methylprednisolone sodium succinate daily

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1: AGEP (Euro SCAR score = 8) patients with typical clinical manifestations who require hospitalization and are aged = 18 years old 2: Voluntary participation, patients or family members can sign informed consent forms, and patients can receive treatment and follow-up as required.

Exclusion criteria

Exclusion criteria: 1: Individuals who are allergic or intolerant to the drugs observed in this experiment 2: Severe liver and kidney dysfunction, uncontrolled hypertension or infection 3: Individuals with mental illness, epilepsy, or severe endocrine disorders 4: Pregnant or lactating women, or women preparing for pregnancy

Design outcomes

Primary

MeasureTime frame
Blood routine and biochemistry;Erythema resolution time;

Secondary

MeasureTime frame
Time of first symptom improvement, length of hospital stay, and cessation of pustule formation after;

Countries

China

Contacts

Public ContactChuan Wan

The First Affiliated Hospital, Jiangxi Medical College, Nanchang University

chuanwan@ncu.edu.cn+86 180 7005 2970

Outcome results

None listed

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