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NCT Number: NCT01384058

Effect of Ezetimibe or Simvastatin or Both on Low Densitiy Lipoprotein -Subfractions in Patients With Type 2 Diabetes

It is of interest how ezetimibe alone or in combination with statin may influence atherogenic dense Low Density Lipoprotein (dLDL) in patients with type 2 diabetes mellitus. The primary objective of this study will be whether there is a change of the concentrations of Apolipoprotein B (ApoB) in dLDL from baseline in each of the 3 treatment groups.

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Key information

About this study

The selective cholesterol resorption inhibitor ezetimibe belongs to a new class of cholesterol lowering drugs. It is of interest how ezetimibe alone or in combination with statin may influence atherogenic dense Low Density Lipoprotein (dLDL) in patients with type 2 diabetes mellitus.

The primary objective of this study will be whether there is a change of the concentrations of Apolipoprotein B (ApoB) in dLDL from baseline in each of the 3 treatment groups. The comparison between treatment groups is exploratory due to insufficient power to detect any change between treatments.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • men > 18 and ≤ 75 years
  • post-menopausal women ≤ 75 years (follicle stimulating hormone (FSH) >30 mIU/ml, women > 60 years FSH > 20 mIU/ml )
  • well controlled diabetes mellitus type II (glycohaemoglobin ≤ 8,0 %)
  • LDL-cholesterol ≤ 160 mg/dl
  • LDL-subfractions: concentration of apoB-100 in dLDL (LDL-5 und LDL-6) > 25 mg/dl
  • written informed consent

Exclusion criteria

  • participation in a clinical trial within the last 30 d before screening- visit
  • patient is unable to give written informed consent
  • Body mass index <15 kg/m² and > 35 kg/m²
  • clinical atherosclerotic disease (coronary heart disease, peripheral artery disease, carotid artery disease)
  • malignoma
  • uncontrolled arterial hypertension (>160/>100 mmHg)
  • clinically relevant disease of liver and/or kidneys
  • clinically relevant endocrinally or hematologic problems
  • allergy to study medication (Ezetimibe and/or Simvastatin)
  • alcohol- or drug abuse
  • laboratory: alanine aminotransferase, aspartate aminotransferase, total bilirubin > 3 x ULN, creatine kinase > 5 x ULN
  • Concurrent treatment with potent CYP3A4-inhibitors (e.g. itraconazole, ketoconazole, HIV-protease-inhibitors, erythromycin, clarithromycin, telithromycin und nefazodone)
  • other relevant diseases

Treatment and study plan

ezetimibe

Drug

ezetimibe 10 mg per day for six weeks

Other names: Ezetrol 10 mg

simvastatin

Drug

Simvastatin 20 mg per day for six weeks

Other names: Zocor MSD

Ezetimibe 10/Simvastatin 20

Drug

Ezetimibe 10mg/Simvastatin 20mg per day for six weeks

Other names: Inegy 10/20

Primary outcomes

  1. Change of the concentration of apolipoprotein B (ApoB) in dense Low Densitiy Lipoprotein (dLDL) from baseline with ezetimibe, simvastatin or the combination of both drugs

    Time frame: baseline and 6 weeks

    multicentre, randomized, open-label study investigation in 6-week effect of ezetimibe (10mg/d), simvastatin (20mg/d) or combination of ezetimibe 10mg/simvastatin 20mg/d on concentrations of dLDL separated by preparative gradient ultracentrifugation in patients with type 2 diabetes.

Secondary outcomes

  1. Change of the concentrations of Total Cholesterol

    Time frame: baseline and 6 weeks

  2. Change of the concentrations of Low Densitiy Lipoprotein (LDL) -Cholesterol

    Time frame: baseline and 6 weeks

  3. Change of the concentrations of High Density Lipoprotein (HDL) -Cholesterol

    Time frame: baseline and 6 weeks

  4. Change of the concentrations of triglycerides

    Time frame: baseline and 6 weeks

Sponsors and collaborators

Lead sponsor

University Hospital Freiburg

Other

Collaborators

  • Essex Pharma GmbH

Registry information

Official study title

The Effect of Ezetimibe 10 mg, Simvastatin 20 mg and the Combination of Simvastatin 20 mg Plus 10 mg Ezetimibe on Low Density Lipoprotein (LDL)-Subfractions in Patients With Type 2 Diabetes

Acronym: EZE

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Jun 28, 2011
Registry last updated
Jun 19, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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