Plaque-type Psoriasis Clinical Trial
— PSOOfficial title:
Energy-restricted, n-3 Polysaturated Fatty Acids-rich Diet Improves the Clinical Response to Immuno-modulating Drugs in Obese Patients With Plaque-type Psoriasis: a Randomized Control Clinical Trial.
Verified date | October 2008 |
Source | Federico II University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Italy: Ethics Committee |
Study type | Interventional |
Low-grade systemic inflammation associated with obesity may worsen the clinical course of
psoriasis. Both a low-calorie diet and nutritional supplementation have been shown to have
an impact on the clinical course of psoriasis, including an anti-inflammatory effect of n-3
polyunsaturated fatty acids (PUFAs). This study aimed to assess the effectiveness of an
energy-restricted diet, enriched in n-3 PUFAs and poor in n-6 PUFAs, on metabolic markers
and clinical outcome of obese patients with psoriasis.
Methods: Forty-four obese patients with mild-to-severe plaque-type psoriasis treated with
immuno-suppressive drugs were randomized to assume either their usual diet or an
energy-restricted diet (20 kcal/kg/ideal body weight/day) enriched of n-3 PUFAs (average 2.6
g/d). All patients continued their immuno-modulating therapy throughout the study. End-point
measures included anthropometric, biochemical and clinical parameters at baseline, 3 and 6
months.
Status | Completed |
Enrollment | 44 |
Est. completion date | October 2008 |
Est. primary completion date | October 2008 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - body mass index (BMI) >30 kg/m2, - age =18 years - clinical diagnosis of plaque-type psoriasis, - mild-to-severe psoriasis clinically stable for at least 5 months - no change in psoriasis therapies for at least five months Exclusion Criteria: - diabetes, - malignancy, - history of food intolerance or autoimmune disorders, - patients non-collaborative |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Italy | federico II University | Naples |
Lead Sponsor | Collaborator |
---|---|
Federico II University |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Composite outcome of Metabolic markers | Fasting blood samples were drawn for the following measurements: serum total cholesterol, HDL-cholesterol (HDL-C), LDL-C, triglycerides, fibrinogen and serum glucose. Serum LDL-C concentration was calculated using the Friedewald equation. | 6 months | No |
Primary | Composite outcome of Anthropometric measurements | BMI was calculated as the ratio of body weight to height2 (kg/m2). Waist circumference was measured with an inelastic tape, the subject in standing position, at the level of the umbilicus. According to the National Cholesterol Education Program (NCEP) Adult Treatment Panel III (ATP III) criteria,abdominal obesity was defined as waist circumference =102 cm in men and =88 cm in women | 6 months | No |
Primary | Composite outcome of Clinical assessments | Clinical assessment was based on three separate instruments: Psoriasis Area and Severity Index (PASI), Dermatology Life Quality Index (DLQI), and VAS for subjective itch ratings. The PASI is used for measuring psoriasis severity. The scale evaluates four areas of the body (head/neck, upper limbs, trunk, and lower limbs) for erythema, scaliness and thickness of psoriatic plaques. The PASI score can range from 0 to 72, with higher scores indicating greater severity. The DLQI is a self-rated instrument consisting of ten items related to the ways that skin disease may impact a patient's health-related quality of life (HRQL). Scores are based on six subscales and has a possible range 0 to 30, with 30 corresponding to the worst HRQL. Subjective itch ratings were recorded using a computerized VAS, anchored by the terms "no itching" (0 points) and "severe itching" (10 points). Subjects were asked to respond in terms of their itching "at the present time". |
6 months | No |
Primary | Composite outcome of Dietary assessment | Dietary compliance was evaluated by experienced dietitians trained for this project, using a combination of food diaries, personal interviews and a detailed food-frequency questionnaire that included 130 foods and beverages. Information on diet included weekly frequency of consumption and portion size. Average daily intakes were calculated by using food tables and industry estimates of the n-3 naturally-rich margarine. Total dietary n3 PUFAs refers to the intake of ALA in addition to of long-chain EPA and DHA. | 6 months | No |
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