- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04073810
Residual Inflammation and Plaque Progression Long-term Evaluation (RIPPLE)
July 18, 2024 updated by: Jason Tarkin, University of Cambridge
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.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
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 Type
Observational
Enrollment (Estimated)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cambridge, United Kingdom
- University of Cambridge
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Patients with recent myocardial infarction and medically managed non-culprit coronary artery disease
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Myocardial infarction
Patients with recent MI
|
Coronary 68Ga-DOTATATE PET-MRI or PET-CT at baseline and 3 months
CTCA at baseline and 2 years
Cardiac MRI at 1 year
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
68Ga-DOTATATE PET vs. plaque progression
Time Frame: 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
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
68Ga-DOTATATE PET vs. CTCA-defined plaque morphology
Time Frame: 2 years
|
Comparison of coronary 68Ga-DOTATATE imaging to changes in plaque morphology measured by CTCA
|
2 years
|
|
68Ga-DOTATATE PET vs. intravascular imaging
Time Frame: Baseline
|
Comparison of 68Ga-DOTATATE imaging to plaque morphology defined by high-resolution intravascular imaging performed during invasive coronary angiography
|
Baseline
|
|
68Ga-DOTATATE PET vs. hsCRP
Time Frame: 2 years
|
Comparison of 68Ga-DOTATATE PET to high-sensitivity C-reactive protein
|
2 years
|
|
68Ga-DOTATATE PET vs left ventricular myocardial function
Time Frame: 1 year
|
Comparison of myocardial 68Ga-DOTATATE PET to left ventricular size and function
|
1 year
|
|
68Ga-DOTATATE PET vs myocardial tissue characterization
Time Frame: 1 year
|
Comparison of myocardial 68Ga-DOTATATE PET to myocardial scarring and oedema
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jason M Tarkin, MBBS PhD, University of Cambridge
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Tarkin JM, Joshi FR, Evans NR, Chowdhury MM, Figg NL, Shah AV, Starks LT, Martin-Garrido A, Manavaki R, Yu E, Kuc RE, Grassi L, Kreuzhuber R, Kostadima MA, Frontini M, Kirkpatrick PJ, Coughlin PA, Gopalan D, Fryer TD, Buscombe JR, Groves AM, Ouwehand WH, Bennett MR, Warburton EA, Davenport AP, Rudd JH. Detection of Atherosclerotic Inflammation by 68Ga-DOTATATE PET Compared to [18F]FDG PET Imaging. J Am Coll Cardiol. 2017 Apr 11;69(14):1774-1791. doi: 10.1016/j.jacc.2017.01.060.
- Pedersen SF, Sandholt BV, Keller SH, Hansen AE, Clemmensen AE, Sillesen H, Hojgaard L, Ripa RS, Kjaer A. 64Cu-DOTATATE PET/MRI for Detection of Activated Macrophages in Carotid Atherosclerotic Plaques: Studies in Patients Undergoing Endarterectomy. Arterioscler Thromb Vasc Biol. 2015 Jul;35(7):1696-703. doi: 10.1161/ATVBAHA.114.305067. Epub 2015 May 14.
- Rominger A, Saam T, Vogl E, Ubleis C, la Fougere C, Forster S, Haug A, Cumming P, Reiser MF, Nikolaou K, Bartenstein P, Hacker M. In vivo imaging of macrophage activity in the coronary arteries using 68Ga-DOTATATE PET/CT: correlation with coronary calcium burden and risk factors. J Nucl Med. 2010 Feb;51(2):193-7. doi: 10.2967/jnumed.109.070672. Epub 2010 Jan 15.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2020
Primary Completion (Estimated)
December 1, 2024
Study Completion (Estimated)
April 1, 2025
Study Registration Dates
First Submitted
August 27, 2019
First Submitted That Met QC Criteria
August 27, 2019
First Posted (Actual)
August 29, 2019
Study Record Updates
Last Update Posted (Actual)
July 19, 2024
Last Update Submitted That Met QC Criteria
July 18, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- A095007 (RIPPLE)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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