RIPPLE: Residual Inflammation and Plaque Progression Long-term Evaluation

Sponsor
University of Cambridge (Other)
Overall Status
Recruiting
CT.gov ID
NCT04073810
Collaborator
Cambridge University Hospitals NHS Foundation Trust (Other), Wellcome Trust (Other)
40
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36
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Study Details

Study Description

Brief Summary

Inflammation drives atherosclerotic plaque rupture triggering most acute coronary syndromes. Despite advances in diagnosis and management of atherosclerosis, patients with myocardial infarction (MI) remain at increased risk of recurrent events. The RIPPLE study aims to examine the relationship between residual coronary inflammation detected by 68Ga-DOTATATE PET in patients treated for MI to long-term plaque progression measured by CT coronary angiography (CTCA). The association between infarct-related myocardial 68Ga-DOTATATE PET and myocardial function and viability will also be assessed.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: PET imaging
  • Diagnostic Test: Coronary CT angiography
  • Diagnostic Test: Cardiac MRI

Detailed Description

While vascular inflammation can be detected using 18F-FDG PET, this method lacks inflammatory cell specificity and is unreliable for coronary imaging because of high background signals from the myocardium. Upregulation of somatostatin receptor subtype-2 (SST2) occurs in activated macrophages, offering a novel inflammation imaging target. 68Ga-DOTATATE, an SST2 PET tracer with low myocardial binding, shows promise for imaging coronary inflammation. Having previously demonstrated increased 68Ga-DOTATATE signals in coronary atherosclerotic lesions post-MI, we now aim to study the natural history of residual arterial inflammation in non-culprit arteries and better understand how 68Ga-DOTATATE signals relate to plaque morphology, progression and rupture. Residual infarct-related myocardial inflammation and its association with ischemic myocardial remodelling will also be examined.

Study Design

Study Type:
Observational
Anticipated Enrollment :
40 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Residual Inflammation and Plaque Progression Long-term Evaluation
Actual Study Start Date :
Oct 1, 2020
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Oct 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Myocardial infarction

Patients with recent MI

Diagnostic Test: PET imaging
Coronary 68Ga-DOTATATE PET-MRI or PET-CT at baseline and 3 months

Diagnostic Test: Coronary CT angiography
CTCA at baseline and 2 years

Diagnostic Test: Cardiac MRI
Cardiac MRI at 1 year

Outcome Measures

Primary Outcome Measures

  1. 68Ga-DOTATATE PET vs. plaque progression [2 years]

    Comparison of non-culprit coronary artery 68Ga-DOTATATE tissue-to-blood ratio at 12 weeks post-MI in patients with plaque progression (changes in low attenuation plaque volume and total atheroma volume) after 2 years measured by CTCA versus those without

Secondary Outcome Measures

  1. 68Ga-DOTATATE PET vs. CTCA-defined plaque morphology [2 years]

    Comparison of coronary 68Ga-DOTATATE imaging to changes in plaque morphology measured by CTCA

  2. 68Ga-DOTATATE PET vs. intravascular imaging [Baseline]

    Comparison of 68Ga-DOTATATE imaging to plaque morphology defined by high-resolution intravascular imaging performed during invasive coronary angiography

  3. 68Ga-DOTATATE PET vs. hsCRP [2 years]

    Comparison of 68Ga-DOTATATE PET to high-sensitivity C-reactive protein

  4. 68Ga-DOTATATE PET vs left ventricular myocardial function [1 year]

    Comparison of myocardial 68Ga-DOTATATE PET to left ventricular size and function

  5. 68Ga-DOTATATE PET vs myocardial tissue characterization [1 year]

    Comparison of myocardial 68Ga-DOTATATE PET to myocardial scarring and oedema

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 99 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male or female participants >18 years old

  • Able to give written, informed consent and to lie flat

  • First-presentation of myocardial infarction within ~2 weeks

  • At least mild non-culprit coronary artery disease on angiography, managed medically

Exclusion Criteria:
  • Women of child bearing potential not using adequate contraception

  • Contrast allergy or contrast-nephropathy

  • Uncontrolled atrial fibrillation

  • Chronic kidney disease (eGFR <30 mL/min/1.73 m2)

  • Any medical condition, in the opinion of the investigator, that prevents the participant from lying flat during scanning, or from participating in the study

  • Uncontrolled chronic inflammatory disorder

  • History of recent malignancy deemed relevant to the study by the investigator

  • Current use of systemic corticosteroids

  • Previous coronary artery bypass grafting surgery (CABG) or percutaneous coronary intervention (PCI) before the index event

  • Contraindication to coronary angiography

  • Requires CABG or staged non-culprit artery PCI

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Cambridge Cambridge United Kingdom

Sponsors and Collaborators

  • University of Cambridge
  • Cambridge University Hospitals NHS Foundation Trust
  • Wellcome Trust

Investigators

  • Principal Investigator: Jason M Tarkin, MBBS PhD, University of Cambridge

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jason Tarkin, Wellcome Clinical Research Career Development Fellow & Clinical Lecturer, University of Cambridge
ClinicalTrials.gov Identifier:
NCT04073810
Other Study ID Numbers:
  • A095007 (RIPPLE)
First Posted:
Aug 29, 2019
Last Update Posted:
Apr 1, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 1, 2022