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Pediatric Atorvastatin in Diabetes Intervention Trial (PADIT)

This study has been completed.

Sponsored by: University of Florida
Information provided by: University of Florida
ClinicalTrials.gov Identifier: NCT00130481
  Purpose

The purpose of this study is to determine if Atorvastatin can improve blood vessel stiffness and blood vessel function in children 10-18 years old with Type 1 and Type 2 diabetes. Subjects will receive atorvastatin 20mg or placebo daily for 3 months and will then switch therapies for the next 3 months.

Hypothesis: Atorvastatin will improve blood vessel function by decreasing arterial stiffness and improving blood flow.


Condition Intervention
Type 1 Diabetes Mellitus
Type 2 Diabetes Mellitus
Drug: Atorvastatin 20 mg daily for 3 months

MedlinePlus related topics:   Diabetes    Diabetes Type 1   

ChemIDplus related topics:   Atorvastatin    Atorvastatin calcium   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Prevention, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Efficacy Study
Official Title:   Pediatric Atorvastatin in Diabetes Intervention Trial (PADIT)

Further study details as provided by University of Florida:

Primary Outcome Measures:
  • Augmentation Index (arterial stiffness)
  • ENDO-PAT (Peripheral Arterial Tone) score (endothelial function)
  • Low density lipoprotein

Secondary Outcome Measures:
  • Urine microalbumin
  • Pubertal stage
  • Body mass index (BMI)
  • Blood pressure
  • Glycated hemoglobin (HbA1c)

Estimated Enrollment:   100
Study Start Date:   April 2005
Study Completion Date:   April 2007

  Eligibility
Ages Eligible for Study:   10 Years to 18 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Type 1 Diabetes Mellitus (T1DM) or Type 2 Diabetes Mellitus (T2DM) for more than 1 year
  • Age 10-18 years.

Exclusion Criteria:

  • Cardiovascular disease (CVD)
  • Liver disease
  • Pregnancy
  • Use of cholesterol or triglyceride lowering drugs
  • Perceived inability to comply with the study protocol
  • Endocrinopathy other than diabetes
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00130481

Locations
United States, Florida
University of Florida    
      Gainesville, Florida, United States, 32610

Sponsors and Collaborators
University of Florida

Investigators
Principal Investigator:     Michael J Haller, MD     University of Florida    
  More Information


Publications:

Study ID Numbers:   576-2004, GCRC M-01 RR 000082, Pfizer 2004-0926, DARE 187
First Received:   August 12, 2005
Last Updated:   April 23, 2007
ClinicalTrials.gov Identifier:   NCT00130481
Health Authority:   United States: Institutional Review Board

Keywords provided by University of Florida:
Diabetes  
Children  
Adolescents  
Arterial Compliance  
Physiology Cardiovascular Endothelium  

Study placed in the following topic categories:
Autoimmune Diseases
Metabolic Diseases
Diabetes Mellitus, Type 1
Diabetes Mellitus, Type 2
Diabetes Mellitus
Endocrine System Diseases
Endocrinopathy
Metabolic disorder
Glucose Metabolism Disorders
Atorvastatin

Additional relevant MeSH terms:
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Immune System Diseases
Therapeutic Uses
Antilipemic Agents
Enzyme Inhibitors
Anticholesteremic Agents
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Pharmacologic Actions

ClinicalTrials.gov processed this record on October 03, 2008




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