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Search / Trial NCT01527097

Influence of Atorvastatin on Psoriasis Severity and Endothelial Function

Launched by SHMUEL FUCHS · Feb 3, 2012

Trial Information

Current as of May 05, 2025

Withdrawn

Keywords

Cardiovascular Diseases Pharmacologic Actions Endothelial Function Dermatology Inflammatory Disease Skin Disease

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients older than 20 years
  • Patients with psoriasis of at least 3-years duration
  • Current moderate to severe psoriatic disease (PASI ≥12, IGA≥3)
  • Statin-naïve patients
  • No history of cardiovascular disease (ischemic heart disease, peripheral vascular disease or cerebrovascular disease)
  • LDL levels
  • LDL level \> 70 mg% and \< 160 mg% in low risk patients (defined as having none or a single risk factor\*)
  • LDL \> 70 mg% and \< 130 mg% in moderate risk patients (defined as the presence of 2 or more risk factors\*)
  • LDL \> 70 mg% and \< 100 mg% in patients with type II diabetes
  • hsCRP ≥ 1 mg/l \* Risk factors: smoking, hypertension (blood pressure \> 140/90 or current treatment with blood pressure lowering agents, HDL \< 40 mg%, family history of premature coronary artery disease in a first degree relative younger than 45 (men) or 55 (women) and obesity (BMI ≥ 30).
  • Exclusion Criteria:
  • Current statin therapy
  • Patents with Atrial Fibrillation
  • Elevated liver enzymes (\> X3 ULN)
  • History of statin-induced liver enzyme elevation
  • Elevated CPK levels (\> X3 ULN)
  • History of myopathy including statin-induced
  • Severe chronic renal failure (GFR \<30 ml/min)
  • Pregnant or breast-feeding women
  • Individuals at risk for poor protocol, or medication compliance
  • Patients with life-expectancy of less than 2 years
  • Patients who are currently participating in another clinical trial
  • Other current active inflammatory and/or infectious conditions
  • Sensitivity to any of atorvastatin ingredients
  • Concomitant drug therapy, taken on a regular basis, which may interact with Atorvastatin

About Shmuel Fuchs

Shmuel Fuchs is a dedicated clinical trial sponsor with a commitment to advancing medical research and improving patient outcomes. With a focus on innovative therapies and evidence-based practices, Shmuel Fuchs oversees a diverse portfolio of clinical studies aimed at addressing unmet medical needs across various therapeutic areas. By prioritizing ethical standards and regulatory compliance, the organization fosters collaboration among researchers, healthcare professionals, and regulatory bodies to ensure the integrity and success of clinical trials. Shmuel Fuchs is dedicated to enhancing the landscape of healthcare through rigorous scientific inquiry and a patient-centered approach.

Locations

Petach Tikva, , Israel

Patients applied

0 patients applied

Trial Officials

Shmuel Fuchs, Professor

Study Director

Rabin Medical Center, Israel

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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