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treatment of palmar psoriasis by methotrexate solution

Iontophoretic delivery of methotrexate in the treatment of palmar psoriasis;a randomized controlled study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/09/009803
Enrollment
50
Registered
2017-09-15
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: L408- Other psoriasis Health Condition 2: null- palmoplantar psoriasis

Interventions

Intervention1: 25 patients will be treated with topical methotrexate solution delivered by iontophoretic device and another 25 patients with clobetasol propionate ointment: evaluate the efficacy of io

Sponsors

Hassan institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Palmoplantar psoriasis patients of more than 18 years of age, with lesions preferably on palms but not involving more than 10% surface area of soles and not involving more than 5% of other body surface area. 2) Patients who are not on systemic anti-psoriatic medication for atleast one month or topical anti-psoriatic medication for atleast 15 days prior to the study. 3) Patients who are willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1) Palmoplantar pustular psoriasis patients. 2) Pregnant and lactating women. 3) Female patients of child bearing potential who cannot be convinced of the need of contraception during and 4 months subsequent to the conclusion of study. 4) Patients with cardiac pace makers or orthopedic implants in the extremities. 5) Patients having haematological abnormality, hepatic and renal dysfunction. 6) Patients having any infection of palms and soles.

Design outcomes

Primary

MeasureTime frame
improvement in modified Palmo Plantar Pustular Psoriasis Area and Severity Index (m-PPPASI)Timepoint: after 6 weeks of treatment

Secondary

MeasureTime frame
adverse effects of treatment and recurrenceTimepoint: follow up for 6 weeks after treatment

Countries

India

Contacts

Public ContactDr Naveen Kumar A C

Hassan institute of medical sciences

dr.ravikumarbc@gmail.com9448742905

Outcome results

None listed

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