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Studying how Cyclosporine affects daily life and safety in people with moderate to severe psoriasis, a short-term hospital study.

Evaluation of quality of life outcomes and safety of Cyclosporine therapy in patients with moderate to severe plaque psoriasis. A prospective, single arm study - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/095862
Enrollment
58
Registered
2025-10-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-10-13

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: nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil

Sponsors

Department of Health Research under MoHFW
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with confirmed diagnosis of moderate to severe plaque psoriasis by a dermatologist, requiring cyclosporine for management as adjudicated by dermatologist 2. Patients with completed age between 18-65 years (both inclusive) of either gender 3. Patients willing to stay adherent to treatment

Exclusion criteria

Exclusion criteria: 1. Patients with pustular, erythrodermic, and/or guttate forms of psoriasis (non-plaque forms of psoriasis) 2. Any reason as per the judgement of the dermatologist which may cause any harm to the patient by cyclosporine treatment 3. Patient not willing to give written informed consent 4. Patients which are half medicated. 5. patients who had previously taken cyclosporine

Design outcomes

Primary

MeasureTime frame
To evaluate the change in DLQI Scores and EQ5D5L Score in patients of moderate to severe plaque psoriasis from baseline to 12 weeksTimepoint: 12 weeks

Secondary

MeasureTime frame
1)To evaluate the Safety of cyclosporine in patients of moderate to severe plaque psoriasis from baseline to 12 weeks on the basis of lab reports , blood pressure and by recording and evaluating the severity of adverse events by using modified Hartwig and Siegel scale 2) To evaluate the change in EQ5D5L Scale in patients of moderate to severe plaque psoriasis from baseline to 12 weeks Timepoint: 12 weeks

Countries

India

Contacts

Public ContactMrunali Sanjay Dudhe

Government Medical College, Nagpur

aturankar@hotmail.com09552283055

Outcome results

None listed

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