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Feasible study of the effect of irbesartan on psoriasis

Feasible study of the effect of irbesartan on psoriasis - The effect of irbesartan on psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025949
Enrollment
10
Registered
2017-02-01
Start date
2012-10-10
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

psoriasis

Interventions

Administration period is three months. Dosage of irbesartan is 100mg.

Sponsors

Department of Dermatology, Kochi Medical School, Kochi University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Psoriasis patients with hypertension

Exclusion criteria

Exclusion criteria: Minors or adults of imcomplete judgement

Design outcomes

Primary

MeasureTime frame
Assessment of PASI three months after the start of Irbesartan

Secondary

MeasureTime frame
Assessment of PDI three months after the start of Irbesartan

Countries

Japan

Contacts

Public ContactHideki Nakajima

Kochi Medical School Department of Dermatology

nakajima@kochi-u.ac.jp0888802363

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026