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Trial record 4 of 5 for:    21247313 [PUBMED-IDS]

Atherosclerosis in High Risk Population Groups: An Assessment by Magnetic Resonance Imaging

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ClinicalTrials.gov Identifier: NCT02114697
Recruitment Status : Completed
First Posted : April 15, 2014
Last Update Posted : February 26, 2018
Sponsor:
Information provided by (Responsible Party):
John Oshinski, Emory University

Brief Summary:

The goal of this study is to assess a slimy substance that settles/deposits along blood vessel wall. This slimy substance is called plaque. Plaque could be made up of fat, calcium or both. Plaque deposition narrows the vessels. This leads to decreased blood flow to various parts of body. Blood vessels include vessels that supply to heart (coronary), vessels to brain (carotid), vessels to kidneys (renal) and vessels to legs (femoral). Decreased blood flow causes symptoms such as brain stroke, heart attack, leg pain. Similarly individuals at risk of cardiovascular disease can have certain markers elevated in their blood that can be measured by simple blood tests.

High or increased plaque deposition is seen in neck vessels of cancer patients who received radiation to chest or head and neck as part of their cancer treatment. Cancer survivors are at increased risk of plaque development and are therefore called high-risk population. Exercise +/- fat lowering medicine can potentially decrease plaque deposition and statins are one of the several fat lowering medications.


Condition or disease Intervention/treatment Phase
Atherosclerosis Drug: Rosuvastatin Behavioral: Lifestyle modification Phase 4

Detailed Description:

Cardiovascular disease (CVD) and cancer are the leading causes of suffering and death amongst the American population. While an ever-increasing number of cancer survivors have a favorable outcome due to advances in cancer treatment; cancer survivors remain at high risk of developing CVD at an early age. There is scant information available on the pathogenic process that contributes to cardiovascular threat amongst cancer survivors and little is known about the interventions, which may interrupt or decrease the risk of CVD in this population. Importantly, early-subclinical markers may substantially precede clinical markers.

The objective of this project is to accurately determine the constituents and characteristics of atherosclerotic plaques in carotid arteries by magnetic resonance imaging (MRI) techniques in cancer survivors; at different data intervals: before and after administration of treatment (medical and life style modification) and then correlate contrast agent dynamics with serum markers of inflammation and other tests of cardiac or vascular dysfunction, where available.

The proposed study involves 100 asymptomatic patients who received prior chest or head and neck radiation therapy (HNXRT) as part of cancer treatment. MRI data (direct assessment of atherosclerosis) would be correlated with indirect measures of atherosclerosis (blood surrogate markers & metabolomics).

The investigators intend to conduct an initial baseline MRI, blood tests (to correlate with surrogate markers of inflammation) and other tests whenever available of cardiac or vascular dysfunction. This cohort will be followed up with medication and/or life style modification regimen for a period of initially18 months and subsequently at 36 months. A repeat of all baseline studies (MRI and blood tests) would be performed as part of the 18 and 36-month follow-up. The plaque characteristics found at MRI will be correlated with results of blood tests (baseline, 18 and 36 months) and changes in one or both will be the expected end point of the study.


Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 10 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Investigator)
Primary Purpose: Treatment
Official Title: Atherosclerosis in High Risk Population Groups: An Assessment by Magnetic Resonance Imaging
Study Start Date : April 2014
Actual Primary Completion Date : July 2017
Actual Study Completion Date : July 2017

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Active Comparator: Lifesyle modification
Lifestyle modification includes a recommended exercise regimen, a healthy diet and decreasing alcohol intake.
Behavioral: Lifestyle modification
Lifestyle modification includes a recommended exercise regimen, a healthy diet and decreasing alcohol intake for 3 years.

Experimental: Rosuvastatin 20 mg
Rosuvastatin 20 mg once a day orally
Drug: Rosuvastatin
Rosuvastatin 20 mg - drug administered orally, once a day, for the duration of the trial, which is 3 years (to be discontinued on account of unacceptable adverse effects)
Other Name: Crestor




Primary Outcome Measures :
  1. Change in cardiovascular disease confirmed by MRI of carotid arteries [ Time Frame: Baseline, 18 months ]
    Plaque features including plaque volume and complexity will act as surrogate measures for progression of cardiovascular disease.

  2. Change in cardiovascular disease confirmed by MRI of carotid arteries [ Time Frame: Baseline, 36 months ]
    Plaque features including plaque volume and complexity will act as surrogate measures for progression of cardiovascular disease.



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Ages Eligible for Study:   22 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age 22 and above with prior head and neck or chest irradiation
  • Six months or more post head and neck irradiation
  • Documented subclinical cardiovascular disease (inflammatory markers in the serum)
  • Pre-existing plaques [detected by ultrasound, CT or MRI]
  • Asymptomatic major arterial stenosis
  • Not being considered for arterial surgery or endovascular treatment.

Exclusion Criteria:

  • Recurrence of cancer (with or without treatment)
  • Planned surgical or endovascular intervention for revascularization of carotid arteries at the time of enrollment
  • Renal failure
  • eGFR < 45 (calculation based on serum creatinine levels, race, age and gender)
  • Medically unstable or hematologic, renal, or hepatic dysfunction
  • Non-atherosclerotic arterial stenosis (dissection)
  • Presence of stents or external clips that can cause artifacts impairing accurate interpretation of MRI data
  • Contraindications to MRI: cardiac pacemaker, metal implants, metal in eyes, pregnant or nursing women, claustrophobia, allergy to MRI contrast
  • Physical or mental impairment that would limit the patient's ability to comply with the medical instructions or study procedures

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02114697


Locations
United States, Georgia
Emory University
Atlanta, Georgia, United States, 30322
Sponsors and Collaborators
Emory University
Investigators
Principal Investigator: John Oshinski, PhD Emory University

Publications:

Responsible Party: John Oshinski, Associate Professor, Emory University
ClinicalTrials.gov Identifier: NCT02114697     History of Changes
Other Study ID Numbers: IRB00059784
First Posted: April 15, 2014    Key Record Dates
Last Update Posted: February 26, 2018
Last Verified: February 2018

Keywords provided by John Oshinski, Emory University:
Cancer survivorship, cardiovascular disease, stroke, TIA

Additional relevant MeSH terms:
Atherosclerosis
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases
Rosuvastatin Calcium
Anticholesteremic Agents
Hypolipidemic Agents
Antimetabolites
Molecular Mechanisms of Pharmacological Action
Lipid Regulating Agents
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Enzyme Inhibitors