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Weekly methotrexate versus daily isotretinoin to treat moderate-to-severe chronic plaque psoriasis: a comparative study

A Comparison of Efficacy of Isotretinoin with that of Methotrexate in Moderate to Severe Chronic Plaque Psoriasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/010891
Enrollment
44
Registered
2017-12-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Chronic plaque psorisis

Interventions

Intervention1: isotretinoin: isotretinoin 30 daily will be used as intervention Control Intervention1: Methtrexate: Methotrexate 15mg once a week will be used as comparator agent

Sponsors

None
Lead Sponsor
Dr Abhinav
Collaborator
Dr Karaninder S Mehta
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having >10% of body surface area involved by psoriasis and no psoriatic arthritis. 2. Patients having moderate-to-severe chronic plaque psoriasis (defined by a score of at least 6 on the Psoriasis Area-and-Severity Index (PASI). 3. Patients not on any form of systemic antipsoriatic treatment for at least 4 weeks and/or topical treatment for at least 2 weeks prior to the initiation of therapy.

Exclusion criteria

Exclusion criteria: 1. Patients less than 18 years of age. 2. Pregnant and / or lactating females. 3. Patients noncompliant with an effective regimen of contraception. 4. Patients having hepatic or renal impairment, deranged lipid profile, hematologic impairment, any acute infection requiring antimicrobial therapy, uncontrolled hypertension or diabetes mellitus, with BMI >30 or known psychiatric illness. 5. Patients having a history of cancer, including skin cancer or hematologic, cerebral or pulmonary neoplasia. 6. Patients who were alcoholic or had a long history of alcohol intake.

Design outcomes

Primary

MeasureTime frame
The reduction in PASI score was the primary outcome measure.Timepoint: At 2 weeks, 4 weeks, 8 weeks and at 12 weeks follow up.

Secondary

MeasureTime frame
Drug associated adverse effectsTimepoint: At 2 weeks, 4 weeks, 8 weeks and at 12 weeks follow up or as and when these are reported by the patients.

Countries

India

Contacts

Public ContactVikram Mahajan

Dr. R. P. Govt Medical College Kangra (Tanda)

drabhinav.c@gmail.com9418007941

Outcome results

None listed

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