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Clinical Study To Evaluate The Efficacy And Safety Of Psoramit Ointment In patients suffering from mild to moderate Psoriasis

An Open Label Single Arm Clinical Study To Evaluate The Efficacy And Safety Of Psoramit Ointment In patients suffering from mild to moderate Psoriasis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/09/021423
Enrollment
87
Registered
2019-09-26
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: L400- Psoriasis vulgaris

Interventions

Intervention1: Psoramit Ointment: Clean the affected area and then apply the ointment over affected area twice daily for the period of 12 weeks.Topical application Control Intervention1: Not Applicabl

Sponsors

The Himalaya Drug Company
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Subject with symptoms of mild to moderate psoriasis with PASI score Subject diagnosed with Mild to moderate chronic plaque psoriasis with Palmoplantar psoriasis, Guttate psoriasis, Flexural psoriasis Age >18 to 65 years, both male and female subjects. Physician Global Assessment score of Patients willing to sign inform consent document.

Exclusion criteria

Exclusion criteria: Patients with Pustular psoriasis, Erythrodermic psoriasis and psoriatic arthritis Subjects treated with other medications / steroids. Significant medical problems such as uncontrolled hypertension / congestive heart failure or any other medication condition Pregnant & Breast feeding Women. History of ongoing, chronic or recurrent infectious disease / lymphoproliferative disease or history of malignancy of any organ system within the past 5 years. History of Alcohol or smoking abuse.

Design outcomes

Primary

MeasureTime frame
Percentage of population achieving PASI 50 (Psoriasis area-and severity index) at End of study as compared to baseline visit.Timepoint: 12 weeks

Secondary

MeasureTime frame
Improvement in Dermatology Life Quality Index (DLQI) at End of study as compared to Baseline visit. Improvement in Physicianâ??s Global assessment (PGA) scoring at End of Study as compared from baseline Visit. Subjects will be assessed for its safety during the study period.Timepoint: 12 weeks

Countries

India

Contacts

Public ContactDr Srikrishna H A

The Himalaya Drug Company

dr.palani@himalayawellness.com

Outcome results

None listed

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