Psoriasis Clinical Trial
Official title:
Assessing the Efficacy and Safety of Metformin in Treatment of Moderate Psoriasis: A Prospective Randomized Double Blind Controlled Study
Psoriasis vulgaris is a common, chronic, relapsing skin disease characterized by predominant
involvement of skin, nails and joints. Recent advances in its patho-physiology have shifted
the notion of psoriasis from that of a 'disease of the skin' to a 'T-cell mediated systemic
disease'. Better understanding of its pathogenesis and co-morbidities along with the
development of novel therapeutics like biological response modifiers has changed the way
dermatologists approach the management of psoriasis. Based on the extent of involvement and
effect on the quality of life, psoriasis may be mild to moderate in severity. This in turn
forms the basis of treatment in majority of the patients. Topical therapies like coal tar,
calcipotriol and corticosteroids are sufficient for mild and localized psoriasis. In more
widespread or severe forms that are associated with significant decrease in quality of life
of patient, phototherapy and systemic therapies are indicated either alone or in combination
with each other. Although the introduction of biological therapies has revolutionized the
treatment of psoriasis in recent years, such newer therapeutic options continue to elude the
vast majority of patients in the developing and under developed world where the traditional
agents like methotrexate, cyclosporine, acitretin and phototherapy still form the backbone
of treatment.
The association of psoriasis with metabolic syndrome is now well documented. Metabolic
syndrome is a cluster of risk factors including central obesity, atherogenic dyslipidemia,
hypertension and glucose intolerance and is a strong predictor of cardiovascular diseases,
diabetes and stroke. Metformin, an oral hypoglycemic agent of biguanide class is known for
its multitude of action on various facets of metabolic syndrome. Recently it has also been
found to inhibit keratinocyte proliferation in cell culture model of psoriasis.
The present study is designed as a randomized controlled double blind pilot study in which
40 patients with chronic plaque psoriasis of moderate severity (PASI ≥ 6 or DLQI ≥ 6) and
metabolic syndrome (By modified ATP III criteria)4 or impaired glucose tolerance (defined as
two-hour glucose levels of 140 to 199 mg per dL on the 75-g oral glucose tolerance test)
will be recruited and randomized into two arms, A and B of 20 each, by using random number
tables. Patients in arm A will be treated with topical anti-psoriatic treatment (including
coal tar and vitamin D3 analogues only) and oral metformin 1g/day 850mg twice daily and
patients in arm B will be treated with topical anti-psoriatic treatment and oral placebo
tablets. Post randomization patients will be followed up at regular intervals for 24 weeks.
During each visit, patients in both arms will be assessed for the severity of psoriasis by
psoriasis activity severity index (PASI) and body mass index (BMI). Fasting blood glucose
and insulin level, glycosylated haemoglobin (HbA1c) and parameters of metabolic syndrome
(including waist circumference, fasting lipid profile and blood pressure) will be assessed
at baseline and again at week 16 and 24. The primary aim of this study is to assess the
efficacy and safety of oral metformin as an add on therapy for the treatment of chronic
plaque psoriasis of moderate severity. The secondary aim is to assess the effect of
metformin on parameters of the metabolic syndrome.
n/a
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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