Research for long term prognosis of severe cutaneous adverse reaction

Research for long term prognosis of severe cutaneous adverse reaction - Research for long term prognosis of severe cutaneous adverse reaction

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000009452

Enrollment

Registered

2012-12-01

Start date

2012-11-15

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

severe cutaneous adverse reaction

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The severe cutaneous adverse reaction patients who administered in our hospital will be involved.

Exclusion criteria

Exclusion criteria: The severe cutaneous adverse reaction patients who administered in our hospital, but still visiting our department will be excluded.

Design outcomes

Primary

Measure	Time frame
Long term prognosis of severe cutaneous adverse reaction will be assessed.	—

Countries

Japan

Contacts

Public ContactHiroaki Azukizawa

Osaka University, Graduate School of Medicine Dermatology

azukizaw@derma.med.osaka-u.ac.jp06-6879-3031

Outcome results