Coronary Artery DiseaseNCT02073617
Aortic Valve and Root Measurements Under Real-Time 3-Dimensional Visualization During Angiography
A study testing Real-time 3-dimensional DynaCT in people with Coronary Artery Disease and Aortic Stenosis, run by NYU Langone Health at 1 site in United States.
Trial summary
The American College of Cardiology/American Heart Association guidelines place symptomatic severe Aortic Stenosis as a class I indication for aortic valve replacement. With the recently approved Edwards-Sapien TAVR device and the ongoing investigations using the CoreValve TAVR device, patients ineligible or at high… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Coronary Artery Disease, Aortic Stenosis
- What is being tested?
- Real-time 3-dimensional DynaCT
- Type of treatment
- Injection or infusion, Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 25 participants
- Where
- 1 siteUnited States
- Study dates
- 6 Jan 2014to 13 Jun 2017
- Phase
- Interventional
- 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
Who may be able to join
- Subjects must be more than 18 years of age with a plan to undergo TAVR.
Who cannot join
- Subjects will be excluded if they meet one of the following criteria:
- estimated glomerular filtration rate <40 mL/min/1.73m2;
- highly irregular heart rates, frequent extra systoles, additional extra pulsations, not in sinus heart rhythm;
- allergy to contrast media;
- pregnant; or
- Unable to consent.
Trial locations and contacts
1 site in 1 country.
United States1 site
NYU Langone Medical Center
New York, New York, 10016
About this study
The American College of Cardiology/American Heart Association guidelines place symptomatic severe Aortic Stenosis as a class I indication for aortic valve replacement. With the recently approved Edwards-Sapien TAVR device and the ongoing investigations using the CoreValve TAVR device, patients ineligible or at high risk for open-heart surgery are now eligible to undergo TAVR.
Patients selected for TAVR undergo an EKG-gated cardiac Multislice CTA to evaluate aortic valve anatomy and aortic root dimensions for device sizing, as well as coronary angiography to define coronary anatomy. Both tests utilize contrast media to visualize anatomy, which may result in contrast-induced nephropathy in anywhere from 7.5% to more than 50% of patients depending on associated clinical risk factors.
Read more
There is a need to consolidate this pre-operative testing whenever possible, and with real-time 3-dimensional visualization of aortic valve and root anatomy using DynaCT cardiac acquisition in the cath lab angiography suite during the coronary angiography, there may be a benefit with reduced contrast load (20 to 35cc for DynaCT, 100cc for CTA).
We would like to make a comparison of aortic valve and root measurements using CTA and DynaCT to affirm the accuracy of DynaCT vs the CTA gold standard.
Read the detailed description
Calcific or degenerative aortic valve disease is one of the most common valvular diseases among the elderly and, with life expectancy continuing to increase, a major source of burden on current healthcare. Although patients with aortic stenosis (AS) can remain asymptomatic for a prolonged period, they do eventually develop symptoms, including angina, exertional syncope and heart failure, which is associated with a 5-year, 3-year, and 1-year, respectively, 50% mortality. The American College of Cardiology/American Heart Association guidelines place symptomatic severe AS as a class I indication for aortic valve replacement. Currently, surgical replacement of the aortic valve is the standard of care. However, with the recently approved Edwards-Sapient TAVR device and the ongoing investigations using the CoreValve TAVR device, patients ineligible or at high risk for open-heart surgery are now eligible to undergo TAVR.
Currently, patients selected for TAVR undergo an EKG-gated cardiac Multislice CTA to evaluate aortic valve anatomy and aortic root dimensions for device sizing. Patients also undergo coronary angiography to define coronary anatomy. Both tests utilize contrast media to visualize anatomy, which may result in contrast-induced nephropathy in anywhere from 7.5% to more than 50% of patients depending on associated clinical risk factors. Contrast-induced nephropathy can, in turn, lead to dialysis and/or increased mortality.
There is a need to consolidate this pre-operative testing whenever possible, and with real-time 3-dimensional visualization of aortic valve and root anatomy using DynaCT cardiac acquisition in the cath lab angiography suite during the coronary angiography, there may be a benefit with reduced contrast load (20 to 35cc for DynaCT, 100cc for CTA). DynaCT conducts fully automatic aortic root segmentation and overlays 3-dimensional structures onto 2-dimensional fluoroscopy in a few seconds (~5 seconds, 60 frames/second rotational angiography). The software automatically recognizes and represents the aortic root, detects and indicates coronary ostia and lowest cusp points of aortic valve (nadir points), and reconstructs commissure lines of aortic valve. Due to cardiac motion, 3-dimensional images without motion correction or cardiac gating will look blurred. Therefore, DynaCT reconstruction motion correction software will be used. The DynaCT motion correction software is a new algorithm that will correct for this motion and apply it during reconstruction- allowing the user to spin without using rapid pacing. However, first, a comparison of aortic valve and root measurements using CTA and DynaCT must be made to affirm the accuracy of DynaCT vs the CTA gold standard.
Study Design This is a pilot study evaluating patients undergoing TAVR at the New York University (NYU) Langone Medical Center. Patients will undergo the standard CTA protocol and invasive coronary angiography performed as part of the pre-operative assessment for TAVR. However, patients in this study will also undergo DynaCT during coronary angiography, utilizing 1 acquisition sweep and 20 to 35cc more of contrast media. Measurements of the major aortic annulus diameter, orthogonal minor aortic annulus diameter, aortic annulus perimeter, maximum ascending aorta diameter at 40mm above the annulus, sinus of Valsalva diameters, sinus of Valsalva heights, and aortic root angulation will be made using both the CTA and DynaCT protocols by a radiologist blinded to patient identity after the study has reached its target recruitment. Based on these measurements, a trained interventional cardiologist will select the appropriate TAVR size in a similarly blinded fashion after the study has reached its target recruitment (i.e. the data collected using DynaCT will not be used in the clinical decision making process). Data will be compared from both modalities using appropriate tests of reproducibility and correlation.
Study Technique CTA will be performed per standard methods as part of standard pre-TAVR evaluation.
Coronary angiography will be performed via femoral artery access (minimum 6Fr) as per standard pre-TAVR evaluation. After coronary angiography is performed, a 6Fr pigtail catheter will be placed in the aorta and 40cc of 50% contrast media diluted normal saline will be delivered using standard automated injection during dynaCT cardiac image acquisition. Intravenous delivery of contrast was considered as alternative.
As per standard care, intravenous access will be obtained and participants will be hydrated during the CTA, coronary angiography, and dynaCT procedures.
- Conditions
- Coronary Artery Disease, Aortic Stenosis
- Being tested
- Real-time 3-dimensional DynaCT
- Keywords
- DynaCT, Aortic valve and root measurements, TAVR
- Medical subject headings
- Coronary Artery Disease, Aortic Valve Stenosis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Real-time 3-dimensional DynaCTRadiation
After coronary angiography is performed, a 6Fr pigtail catheter will be placed in the aorta and 40cc of 50% contrast media diluted normal saline will be delivered using standard automated injection during dynaCT cardiac image acquisition. Intravenous delivery of contrast as alternative.
| Study group | Role | What they receive |
|---|---|---|
| Real-time 3-dimensional DynaCT | Experimental | Patients will undergo the standard CTA protocol and invasive coronary angiography performed as part of the pre-operative assessment for TAVR. Patients in this study will also undergo DynaCT during coronary angiography, utilizing 1 acquisition sweep and 20 to 35cc more of contrast media. Measurements of the major aortic annulus diameter, orthogonal minor aortic annulus diameter, aortic annulus perimeter, maximum ascending aorta diameter at 40mm above the annulus, sinus of Valsalva diameters, sinus of Valsalva heights, and aortic root angulation will be made using both the CTA and DynaCT protocols by a radiologist blinded to patient identity. Based on these measurements, a trained interventional cardiologist will select the appropriate TAVR size for the patient. Receives: Radiation: Real-time 3-dimensional DynaCT |
What is being measured
The primary outcome is the main question the study is designed to answer.
Correlation of aortic annulus measurement measured on invasive 3D dyna CT (experimental) and on non-invasive CT scan (standard of care)
Each patient will undergo non-invasive CT scan for aortic annulus measurement (in order to choose appropriate TAVR size) as per standard of care. They will then undergo invasive dyna CT for aortic annulus measurement during their clinically-indicated invasive coronary angiogram. The primary outcome is correlation between the aortic annulus dimension measurement made on dyna CT and non-invasive CT.
Measured: 1 day
Secondary outcomes (1)
TAVR size
A trained interventional cardiologist will evaluate the measurements made from each CTA abd DynaCT image and select the appropriate TAVR size in a blinded fashion.
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Feb 2014 (estimated)
- Study start6 Jan 2014
- Primary completion22 Jun 2016
- Study completion13 Jun 2017
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.
- More trials run by NYU Langone HealthThe sponsor's other registered studies.
- 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 25 participants (actual)
Sponsor and investigators
- Lead sponsor
- NYU Langone Health
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Binita Shah, MD, MS, Principal investigator, NYU Langone Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02073617
- Sponsor's protocol ID
- 13-00804
- Status last verified
- Jul 2017
- First submitted
- 19 Feb 2014
- Last updated
- 18 Jul 2017
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Jul 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Aortic Valve and Root Measurements Under Real-Time 3-Dimensional Visualization During Angiography
- ClinicalTrials.gov ID
- NCT02073617
- Acronym / sponsor ID
- 13-00804
- Conditions
- Coronary Artery Disease, Aortic Stenosis
- Keywords
- DynaCT, Aortic valve and root measurements, TAVR
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 25 participants (actual)
- Lead sponsor
- NYU Langone HealthUniversity, hospital or other
- Study start
- 6 Jan 2014 (actual)
- Primary completion
- 22 Jun 2016 (actual)
- Study completion
- 13 Jun 2017 (actual)
- First posted
- 27 Feb 2014 (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 American College of Cardiology/American Heart Association guidelines place symptomatic severe Aortic Stenosis as a class I indication for aortic valve replacement. With the recently approved Edwards-Sapien TAVR device and the ongoing investigations using the CoreValve TAVR device, patients ineligible or at high risk for open-heart surgery are now eligible to undergo TAVR.
Patients selected for TAVR undergo an EKG-gated cardiac Multislice CTA to evaluate aortic valve anatomy and aortic root dimensions for device sizing, as well as coronary angiography to define coronary anatomy. Both tests utilize contrast media to visualize anatomy, which may result in contrast-induced nephropathy in anywhere from 7.5% to more than 50% of patients depending on associated clinical risk factors.
There is a need to consolidate this pre-operative testing whenever possible, and with real-time 3-dimensional visualization of aortic valve and root anatomy using DynaCT cardiac acquisition in the cath lab angiography suite during the coronary angiography, there may be a benefit with reduced contrast load (20 to 35cc for DynaCT, 100cc for CTA).
We would like to make a comparison of aortic valve and root measurements using CTA and DynaCT to affirm the accuracy of DynaCT vs the CTA gold standard.
Detailed description
Calcific or degenerative aortic valve disease is one of the most common valvular diseases among the elderly and, with life expectancy continuing to increase, a major source of burden on current healthcare. Although patients with aortic stenosis (AS) can remain asymptomatic for a prolonged period, they do eventually develop symptoms, including angina, exertional syncope and heart failure, which is associated with a 5-year, 3-year, and 1-year, respectively, 50% mortality. The American College of Cardiology/American Heart Association guidelines place symptomatic severe AS as a class I indication for aortic valve replacement. Currently, surgical replacement of the aortic valve is the standard of care. However, with the recently approved Edwards-Sapient TAVR device and the ongoing investigations using the CoreValve TAVR device, patients ineligible or at high risk for open-heart surgery are now eligible to undergo TAVR.
Currently, patients selected for TAVR undergo an EKG-gated cardiac Multislice CTA to evaluate aortic valve anatomy and aortic root dimensions for device sizing. Patients also undergo coronary angiography to define coronary anatomy. Both tests utilize contrast media to visualize anatomy, which may result in contrast-induced nephropathy in anywhere from 7.5% to more than 50% of patients depending on associated clinical risk factors. Contrast-induced nephropathy can, in turn, lead to dialysis and/or increased mortality.
There is a need to consolidate this pre-operative testing whenever possible, and with real-time 3-dimensional visualization of aortic valve and root anatomy using DynaCT cardiac acquisition in the cath lab angiography suite during the coronary angiography, there may be a benefit with reduced contrast load (20 to 35cc for DynaCT, 100cc for CTA). DynaCT conducts fully automatic aortic root segmentation and overlays 3-dimensional structures onto 2-dimensional fluoroscopy in a few seconds (~5 seconds, 60 frames/second rotational angiography). The software automatically recognizes and represents the aortic root, detects and indicates coronary ostia and lowest cusp points of aortic valve (nadir points), and reconstructs commissure lines of aortic valve. Due to cardiac motion, 3-dimensional images without motion correction or cardiac gating will look blurred. Therefore, DynaCT reconstruction motion correction software will be used. The DynaCT motion correction software is a new algorithm that will correct for this motion and apply it during reconstruction- allowing the user to spin without using rapid pacing. However, first, a comparison of aortic valve and root measurements using CTA and DynaCT must be made to affirm the accuracy of DynaCT vs the CTA gold standard.
Study Design This is a pilot study evaluating patients undergoing TAVR at the New York University (NYU) Langone Medical Center. Patients will undergo the standard CTA protocol and invasive coronary angiography performed as part of the pre-operative assessment for TAVR. However, patients in this study will also undergo DynaCT during coronary angiography, utilizing 1 acquisition sweep and 20 to 35cc more of contrast media. Measurements of the major aortic annulus diameter, orthogonal minor aortic annulus diameter, aortic annulus perimeter, maximum ascending aorta diameter at 40mm above the annulus, sinus of Valsalva diameters, sinus of Valsalva heights, and aortic root angulation will be made using both the CTA and DynaCT protocols by a radiologist blinded to patient identity after the study has reached its target recruitment. Based on these measurements, a trained interventional cardiologist will select the appropriate TAVR size in a similarly blinded fashion after the study has reached its target recruitment (i.e. the data collected using DynaCT will not be used in the clinical decision making process). Data will be compared from both modalities using appropriate tests of reproducibility and correlation.
Study Technique CTA will be performed per standard methods as part of standard pre-TAVR evaluation.
Coronary angiography will be performed via femoral artery access (minimum 6Fr) as per standard pre-TAVR evaluation. After coronary angiography is performed, a 6Fr pigtail catheter will be placed in the aorta and 40cc of 50% contrast media diluted normal saline will be delivered using standard automated injection during dynaCT cardiac image acquisition. Intravenous delivery of contrast was considered as alternative.
As per standard care, intravenous access will be obtained and participants will be hydrated during the CTA, coronary angiography, and dynaCT procedures.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Real-time 3-dimensional DynaCT | Experimental | Radiation: Real-time 3-dimensional DynaCTPatients will undergo the standard CTA protocol and invasive coronary angiography performed as part of the pre-operative assessment for TAVR. Patients in this study will also undergo DynaCT during coronary angiography, utilizing 1 acquisition sweep and 20 to 35cc more of contrast media. Measurements of the major aortic annulus diameter, orthogonal minor aortic annulus diameter, aortic annulus perimeter, maximum ascending aorta diameter at 40mm above the annulus, sinus of Valsalva diameters, sinus of Valsalva heights, and aortic root angulation will be made using both the CTA and DynaCT protocols by a radiologist blinded to patient identity. Based on these measurements, a trained interventional cardiologist will select the appropriate TAVR size for the patient. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Subjects must be more than 18 years of age with a plan to undergo TAVR.
Key exclusion criteria (6 listed)
- Subjects will be excluded if they meet one of the following criteria:
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 |
|---|---|---|
| Real-time 3-dimensional DynaCTAfter coronary angiography is performed, a 6Fr pigtail catheter will be placed in the aorta and 40cc of 50% contrast media diluted normal saline will be delivered using standard automated injection during dynaCT cardiac image acquisition. Intravenous delivery of contrast as alternative. | Radiation | Real-time 3-dimensional DynaCT |
Primary outcome
Correlation of aortic annulus measurement measured on invasive 3D dyna CT (experimental) and on non-invasive CT scan (standard of care)
Time frame: 1 day
Each patient will undergo non-invasive CT scan for aortic annulus measurement (in order to choose appropriate TAVR size) as per standard of care. They will then undergo invasive dyna CT for aortic annulus measurement during their clinically-indicated invasive coronary angiogram. The primary outcome is correlation between the aortic annulus dimension measurement made on dyna CT and non-invasive CT.
1 secondary outcome
TAVR size
Time frame: 1 day
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 18 Jul 2017.
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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.
Binita Shah, MD, MS principal investigator
NYU Langone Health
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Real-time 3-dimensional DynaCT in people with Coronary Artery Disease and Aortic Stenosis, run by NYU Langone Health at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 6 exclusion criteria. 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 18 Jul 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
Correlation of aortic annulus measurement measured on invasive 3D dyna CT (experimental) and on non-invasive CT scan (standard of care) (time frame: 1 day). 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 18 Jul 2017.