Coronary Artery DiseaseVERDICTNCT01158053
Vascular Evaluation for Revascularization: Defining the Indications for Coronary Therapy: A Pilot Study
An observational study of Coronary Artery Disease, run by Volcano Corporation.
Trial summary
The present prospective, multicenter study will therefore be performed with the primary objective of establishing the correlation between fractional flow reserve (FFR) and intravascular ultrasound with virtual histology (VH-IVUS)-derived parameters in angiographically intermediate coronary lesions. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Coronary Artery Disease
- What is being tested?
- FFR and VH-IVUS and IVUS and FFR
- Type of treatment
- Medical device
- How many people
- 291 participants
- Where
- No sites listed yet
- Study dates
- Sep 2010to Jan 2015
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: patients scheduled to undergo a diagnostic cardiac catheterization
Patient-specific inclusion criteria:
- Clinical presentation: stable angina, unstable angina, non-ST segment-elevation myocardial infarction (NSTEMI) (Braunwald classification of unstable angina, see Attachment 2) or recent STEMI (>48 hours before enrollment).
- Patient is scheduled for coronary catheterization with or without percutaneous coronary intervention.
- Age ≥18 years.
- Patient is able to read, understand, and sign the informed consent document.
- Patient agrees to all protocol related procedures, including follow-up through 3 years.
Lesion-specific inclusion criteria:
- The patient has at least one intermediate coronary lesion to be assessed by FFR and VH-IVUS, defined as a lesion with a visually-estimated diameter stenosis ≥40% to <80% with a visually-estimated angiographic reference segment diameter of 2.75 mm - 4.0 mm.
- There may only be one study lesion in the major epicardial coronary artery or its branches. All other stenosis in this epicardial coronary artery or its branches must be <40% by visual angiographic assessment. E.g.., if the lesion is in the Left Anterior Descending(LAD), there may be no other significant lesions (≥40%) in the LAD, septals or diagonal branches. A single lesion may have normal or nearly normal appearing segments within the lesion as long as it is contained within one CASS segment. Moreover, a single lesion may span two or more CASS segments as long as there is no normal or nearly normal appearing segments >5mm in length within the lesion. However, if a diseased lesion extends across two or more CASS segments and has one or more >5 mm lengths of normal or nearly normal appearing segments within the lesion, then it is considered 2 separate lesions, and may not be enrolled.
- More than 1 intermediate lesion per patient may be enrolled, as long as each lesion meets the entry criteria as a study lesion (e.g. one intermediate lesion in 1, 2 or 3 unique epicardial coronary arteries (LAD vs. LCX vs. RCA), with FFR and VH-IVUS performed in each vessel. Thus, up to 3 lesions may be enrolled per patient (one in each major epicardial coronary artery).
- PCI of any lesion in the target vessel (the main epicardial coronary artery or any of its branches) may not have been performed in the preceding 1 year (including during the index procedure) and may not be planned within the next 1 year.
- Patients undergoing PCI of non-study lesions in non-study target vessels during the index procedure may be enrolled if one or more qualifying intermediate lesion is otherwise present in a different epicardial vessel, but PCI of all non-study lesions must be performed first (including staged procedures) and must be successful and uncomplicated before formal enrollment into this study. The PCI cannot occur in the epicardial coronary artery or its branches containing the intermediate lesion.
- Successful PCI is defined as residual diameter stenosis of <50% in all treated lesions with Thrombolysis in Myocardial Infarction (TIMI) -3 flow in all treated vessels.
- Uncomplicated PCI is defined as the absence of intra-procedural chest pain or ST-segment changes lasting >10 minutes, sustained vessel closure, slow or no reflow, side branch loss, distal embolization, perforation, residual dissection (>type B), or requirement for cardiopulmonary resuscitation, cardioversion or defibrillation, pacemaker insertion, intubation, intra-aortic balloon insertion or intravenous pressors.
Patient-specific exclusion criteria:
- Prior CABG at any time.
- The patient is likely to undergo PCI, CABG or other cardiac surgical procedure within 1 year of the procedure.
- ST-segment elevation myocardial infarction within 48 hours of the procedure.
- Cardiogenic shock defined as systolic blood pressure <90 mmHg lasting >30 minutes, not responding to intravenous fluids, and/or requiring intravenous pressors or an intra-aortic balloon pump or other hemodynamic support device.
- Heart failure as defined by New York Heart Association class III or IV (see Attachment 2).
- Respiratory failure requiring intubation or supplementary oxygen.
- Left ventricular ejection fraction <30% as determined by 2D echo, nuclear testing, magnetic resonance imaging (MRI), or left ventriculography.
- Any moderate or severe cardiac valve disease.
- Cerebrovascular accident or transient ischemic attack (TIA) within the past 60 days, or any permanent neurologic deficit.
- Chronic renal insufficiency (serum creatinine > 2.5mg/dl).
- History of drug abuse or alcohol abuse or any other condition making it unlikely that the patient will comply with all study procedures, including follow-up for 3 years
- Any condition with expected survival <2 years.
- Pregnant or nursing patients and those who plan pregnancy in the period up to 1 year following the index procedure. Female patients of child-bearing potential must have a negative pregnancy test done within 7 days prior to the index procedure.
- Patients currently participating in another study of an investigational drug or device which has not yet reached its primary endpoint.
- Oral intake by the patient of any caffeinated beverage within 4 hours of the procedure
- Use within 12 hours of theophylline, aminophylline or any xanthine derivative.
Lesion-specific exclusion criteria:
- An unprotected left main coronary stenosis is present (visually assessed %DS ≥40%, whether or not requiring treatment). The study lesion cannot be a left main lesion.
- The intermediate lesion is in a vessel with thrombus, moderate or severe calcification, angulation, or tortuosity. PCI may be performed in such non target vessels or lesions prior to study enrollment, however, as long as successful and uncomplicated, after which the patient is enrolled in the study.
- The study lesion is an ostial lesion (within 5 mm of the aorta or the distal left main coronary artery) or is bifurcation lesion requiring planned dual stenting.
About this study
Official title: A Prospective, Global, Multicenter, Non-Randomized, Non-Blinded Study in Patients With Intermediate Coronary Lesions to Examine the Correlation Between Fractional Flow Reserve (FFR) and Intravascular Ultrasound With Virtual Histology (VH-IVUS)
The present prospective, multicenter study will therefore be performed with the primary objective of establishing the correlation between fractional flow reserve (FFR) and intravascular ultrasound with virtual histology (VH-IVUS)-derived parameters in angiographically intermediate coronary lesions. The current study will also examine the relative prognostic utility of FFR and VH-IVUS as a tool to defer percutaneous coronary intervention (PCI), by assessing the long-term rate (up to 3 years) of lesion-related clinical events if deferred by FFR vs. VH-IVUS versus not deferred PCI.
- Conditions
- Coronary Artery Disease
- Being tested
- FFR and VH-IVUS, IVUS and FFR
- Medical subject headings
- Coronary Artery Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
FFR and VH-IVUSDevice
- Stable Angina(SA), Unstable Angina(UA),Non ST-segment Elevation Myocardial Infarction(NSTEMI) or ST-segment Elevation Myocardial Infarction(STEMI) >48hrs scheduled for cardiac catheterization ± PCI. All patient level inclusion and no exclusion criteria are met Signed Informed Consent
- No PCI or successful and uncomplicated PCI of all non study lesions. One or more study lesions identified.
All lesion level inclusion criteria and no exclusion criteria are met.
- FFR followed by VH-IVUS of study lesion(s)
- Any additional PCI based on routine clinical practice and FFR/IVUS data?
- If Yes: Final IVUS with VH imaging, Clinical follow-up at hospital discharge, 30 days, 6 months, and then yearly for 3 years
- If No: Clinical follow-up at hospital discharge, 30 days, 6 months, and then yearly for 3 years
IVUS and FFRDevice
Also called Eagle Eye IVUS catheter, Prine Wire
What is being measured
The primary outcome is the main question the study is designed to answer.
The concordance between FFR and IVUS minimum lumen area(MLA) as assessed by continuous correlation (regression), categorical cutoff values , and being unadjusted and adjusted for lesion length, %plaque burden(PB) and VH-thin capped Fibro Atheroma(TCFA)
Measured: 3 year
Secondary outcomes (6)
The concordance between operator assessed % diameter stenosis(DS), core lab assessed %DS, FFR and MLA in intermediate lesions
Measured: 3 year
Operator assessed and core lab assessed angiographic %DS, and VH-IVUS MLA, lesion length, %PB, and plaque types in intermediate lesions, with core lab assessment as the reference
Measured: 3 year
FFR and VH-IVUS derived MLA, %PB, lesion length, and plaque type in deferred vs. treated lesions
Measured: 3 year
Operator revascularization decisions (deferral vs. PCI/coronary artery bypass graft(CABG)) according to operator assessed angiographic %DS, FFR and VH-IVUS results in intermediate coronary lesions
Measured: 3 year
Deferred study lesion clinical event rates up to three years according to %DS, FFR and VH-IVUS, and comparison with treated study lesion clinical event rates up to three years
Measured: 3 year
Treated study lesion clinical event rates up to three years and their correlation with index FFR and VH-IVUS pre and post stenting
Measured: 3 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 Jul 2010 (estimated)
- Study startSep 2010
- Primary completionApr 2012
- Study completionJan 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Coronary Artery DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 291 participants (actual)
Sponsor and investigators
- Lead sponsor
- Volcano Corporation
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Gregg W Stone, MD, Principal investigator, Columbia University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01158053
- Sponsor's protocol ID
- RFC-001
- Acronym
- VERDICT
- Status last verified
- Jun 2015
- First submitted
- 22 Jun 2010
- Last updated
- 10 Dec 2015
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 10 Dec 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Prospective, Global, Multicenter, Non-Randomized, Non-Blinded Study in Patients With Intermediate Coronary Lesions to Examine the Correlation Between Fractional Flow Reserve (FFR) and Intravascular Ultrasound With Virtual Histology (VH-IVUS)
- ClinicalTrials.gov ID
- NCT01158053
- Acronym / sponsor ID
- VERDICT / RFC-001
- Conditions
- Coronary Artery Disease
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 291 participants (actual)
- Lead sponsor
- Volcano CorporationIndustry (pharma, biotech, devices)
- Study start
- Sep 2010
- Primary completion
- Apr 2012 (actual)
- Study completion
- Jan 2015 (actual)
- First posted
- 8 Jul 2010 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The present prospective, multicenter study will therefore be performed with the primary objective of establishing the correlation between fractional flow reserve (FFR) and intravascular ultrasound with virtual histology (VH-IVUS)-derived parameters in angiographically intermediate coronary lesions. The current study will also examine the relative prognostic utility of FFR and VH-IVUS as a tool to defer percutaneous coronary intervention (PCI), by assessing the long-term rate (up to 3 years) of lesion-related clinical events if deferred by FFR vs. VH-IVUS versus not deferred PCI.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- patients scheduled to undergo a diagnostic cardiac catheterization
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| FFR and VH-IVUS* Stable Angina(SA), Unstable Angina(UA),Non ST-segment Elevation Myocardial Infarction(NSTEMI) or ST-segment Elevation Myocardial Infarction(STEMI) >48hrs scheduled for cardiac catheterization ± PCI. All patient level inclusion and no exclusion criteria are met Signed Informed Consent * No PCI or successful and uncomplicated PCI of all non study lesions. One or more study lesions identified. All lesion level inclusion criteria and no exclusion criteria are met. * FFR followed by VH-IVUS of study lesion(s) * Any additional PCI based on routine clinical practice and FFR/IVUS data? * If Yes: Final IVUS with VH imaging, Clinical follow-up at hospital discharge, 30 days, 6 months, and then yearly for 3 years * If No: Clinical follow-up at hospital discharge, 30 days, 6 months, and then yearly for 3 years | Device | – |
| IVUS and FFRAlso: Eagle Eye IVUS catheter, Prine Wire | Device | – |
Primary outcome
The concordance between FFR and IVUS minimum lumen area(MLA) as assessed by continuous correlation (regression), categorical cutoff values , and being unadjusted and adjusted for lesion length, %plaque burden(PB) and VH-thin capped Fibro Atheroma(TCFA)
Time frame: 3 year
6 secondary outcomes
The concordance between operator assessed % diameter stenosis(DS), core lab assessed %DS, FFR and MLA in intermediate lesions
Time frame: 3 year
Operator assessed and core lab assessed angiographic %DS, and VH-IVUS MLA, lesion length, %PB, and plaque types in intermediate lesions, with core lab assessment as the reference
Time frame: 3 year
FFR and VH-IVUS derived MLA, %PB, lesion length, and plaque type in deferred vs. treated lesions
Time frame: 3 year
Operator revascularization decisions (deferral vs. PCI/coronary artery bypass graft(CABG)) according to operator assessed angiographic %DS, FFR and VH-IVUS results in intermediate coronary lesions
Time frame: 3 year
Deferred study lesion clinical event rates up to three years according to %DS, FFR and VH-IVUS, and comparison with treated study lesion clinical event rates up to three years
Time frame: 3 year
Treated study lesion clinical event rates up to three years and their correlation with index FFR and VH-IVUS pre and post stenting
Time frame: 3 year
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Dec 2015.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Gregg W Stone, MD principal investigator
Columbia University
Questions about this trial
What is this clinical trial studying?
An observational study of Coronary Artery Disease, run by Volcano Corporation.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Dec 2015. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The concordance between FFR and IVUS minimum lumen area(MLA) as assessed by continuous correlation (regression), categorical cutoff values , and being unadjusted and adjusted for lesion length, %plaque burden(PB) and VH-thin capped Fibro Atheroma(TCFA) (time frame: 3 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Dec 2015.