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Fluvastatin AmelIorates aTHerosclerosis Study (FAITH)

Primary Purpose

Coronary Heart Disease, Atherosclerosis

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Fluvastatin extended release tablet
Sponsored by
Beijing Anzhen Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Heart Disease focused on measuring statin, atherosclerosis, Coronary heart disease, OPN, OPG

Eligibility Criteria

45 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Newly diagnosed coronary heart disease
  2. One or more maximum IMT measurements of ≥1.1mm.
  3. Age 45 to 70 years old
  4. LDL-C≥130mg/dL
  5. Not receiving regular lipid lowering treatment
  6. Written Informed Consent

Exclusion Criteria:

  1. Myocardial infarction as the first symptoms of coronary heart disease
  2. Patients with known hypersensitivity to fluvastatin or any of the excipients
  3. Pregnancy or lactation, or women of childbearing potential not using effective contraception
  4. Known muscle disease or history of muscle disease (e.g. myopathy, myositis, rhabdomyolysis) and/or serum CK levels greater than 2 x upper limit of normal (ULN)
  5. renal dysfunction
  6. Active liver disease and/or serum transaminase levels (ALT, AST) greater than 2x ULN
  7. Any conditions the investigator consider not suitable for long-term follow up

Sites / Locations

  • Cardiology department ,Beijing Anzhen hospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Fluvastatin extended release tablet

Arm Description

Fluvastatin extended release tablet 80mg/day

Outcomes

Primary Outcome Measures

carotid IMT

Secondary Outcome Measures

lipid variables:TC, TG, LDL-C, HDL-C, apo B, apo A-I

Full Information

First Posted
September 5, 2012
Last Updated
September 5, 2012
Sponsor
Beijing Anzhen Hospital
Collaborators
Novartis
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1. Study Identification

Unique Protocol Identification Number
NCT01681199
Brief Title
Fluvastatin AmelIorates aTHerosclerosis Study
Acronym
FAITH
Official Title
The Efficacy of Lescol XL(Fluvastatin Extended Release 80 mg) on Atherosclerosis Progression in Patients With Newly Diagnosed Coronary Heart Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2012
Overall Recruitment Status
Unknown status
Study Start Date
July 2012 (undefined)
Primary Completion Date
April 2014 (Anticipated)
Study Completion Date
August 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing Anzhen Hospital
Collaborators
Novartis

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The study is designed to assess the effect of statin on atherosclesrosis progression as well as to explore its potential mechanism besides lipid modifying , such as effect on inflammation and vascular calcification.
Detailed Description
Carotid IMT has been used in various studies (e.g. ASAP, ARBITER, METEOR) and is well accepted as a valid surrogate marker for atherosclerosis. The thickness of CIMT is significantly associated with the presence and the extent of coronary disease. Slower progression of atherosclerosis as measured by carotid ultrasound is also associated with a lower risk of nonfatal MI. In a meta analysis, for every 0.0 1-mm-per-year decrease in carotid IMT, there was a significant 18% reduction in the risk of nonfatal MI. Measurement of carotid IMT carries the advantage of being non-invasive and easy to use with a good degree of reproducibility. Statins have been shown to slow the progression of atherosclerosis or even to induce regression of atherosclerosis. Change of carotid IMT by statins have been found to correlate with the extent of LDL-C reduction and HDL-C increase however non-lipid effects (e.g. effects on inflammation, calcification ) may also play a role in the beneficial effects of statins on atherosclerosis.Osteopontin (OPN), an acidic phosphoprotein, and osteoprotegerin (OPG), a member of the tumor necrosis factor-a receptor superfamily, have been recently demonstrated to modulate vascular calcification. Recent studies have shown an association of serum OPN and OPG levels with cardiovascular diseases and vulnerable carotid plaque .

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Heart Disease, Atherosclerosis
Keywords
statin, atherosclerosis, Coronary heart disease, OPN, OPG

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
140 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fluvastatin extended release tablet
Arm Type
Experimental
Arm Description
Fluvastatin extended release tablet 80mg/day
Intervention Type
Drug
Intervention Name(s)
Fluvastatin extended release tablet
Other Intervention Name(s)
Lescol XL
Primary Outcome Measure Information:
Title
carotid IMT
Time Frame
1 year
Secondary Outcome Measure Information:
Title
lipid variables:TC, TG, LDL-C, HDL-C, apo B, apo A-I
Time Frame
week 12 and 24
Other Pre-specified Outcome Measures:
Title
hs-CRP, Lp-PLA2, OPN and OPG.
Time Frame
week 12,24 and 52

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newly diagnosed coronary heart disease One or more maximum IMT measurements of ≥1.1mm. Age 45 to 70 years old LDL-C≥130mg/dL Not receiving regular lipid lowering treatment Written Informed Consent Exclusion Criteria: Myocardial infarction as the first symptoms of coronary heart disease Patients with known hypersensitivity to fluvastatin or any of the excipients Pregnancy or lactation, or women of childbearing potential not using effective contraception Known muscle disease or history of muscle disease (e.g. myopathy, myositis, rhabdomyolysis) and/or serum CK levels greater than 2 x upper limit of normal (ULN) renal dysfunction Active liver disease and/or serum transaminase levels (ALT, AST) greater than 2x ULN Any conditions the investigator consider not suitable for long-term follow up
Facility Information:
Facility Name
Cardiology department ,Beijing Anzhen hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100029
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xin Du, PhD
Phone
86 15010519643
Email
duxinheart@sina.com
First Name & Middle Initial & Last Name & Degree
Xin Du, PhD

12. IPD Sharing Statement

Learn more about this trial

Fluvastatin AmelIorates aTHerosclerosis Study

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