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Effect of drug Rosuvastatin When given in addition to the existing treatment in patients of skin disease (chronic plaque psoriasis)

Phase 2
Completed
Conditions
Health Condition 1: L408- Other psoriasis
Registration Number
CTRI/2023/02/049424
Lead Sponsor
Pt BD Sharma PGIMS Rohtak
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
48
Inclusion Criteria

1)Patients having Chronic Plaque Psoriasis with Body surface area involvement of 10 percent or greater

2)Patients who are willing to give written informed consent

Exclusion Criteria

1)Patients with present or past history of clinical atherosclerotic cardiovascular disease

2)Patients having deranged Liver Tunction test(LFT)/ Active liver disease(ALD)

3)Patients having clinical features suggestive of myopathy

4)Patients having known allergy to statins

5)Patients who are already on statins

6)Pregnancy and lactation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Psoriatic Area and Severity Index(PASI) ScoreTimepoint: Baseline, 4 weeks, 8 weeks and 12 weeks
Secondary Outcome Measures
NameTimeMethod
Dermatology Life and Quality Index (DLQI)Timepoint: Baseline and 12 weeks;High sensitivity- C reactive protein (hs-CRP)Timepoint: Baseline and 12 weeks;Lipid ProfileTimepoint: Baseline and 12 weeks;PASI 50Timepoint: At the end of 12 weeks
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