search
Back to results

Comprehensive Cardiothoracic Dual Source CT for the Early Triage of Patients With Acute Chest Pain (CAPTURE)

Primary Purpose

Chest Pain Syndrome

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Comprehensive Cardiothoracic CT arm
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Chest Pain Syndrome

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Males or females >30 years of age in sinus rhythm
  • Willing and able to provide written informed consent
  • Undifferentiated chest discomfort or shortness of breath with a component of chest discomfort within the last 24 hours
  • Intermediate likelihood of MI, pulmonary embolism (PE), or aortic dissection (AD) as determined by ED providers after completion of standard initial clinical evaluation
  • ED providers independently decide that the patient's care plan should include a coronary, PE, or AD CT.
  • Female patients must be either of non-childbearing potential (i.e., surgically sterilized or post menopausal [≥ 12 consecutive months without menses]) or must have a negative pregnancy test

Exclusion Criteria:

  • Positive cardiac biomarkers (elevated serum creatine phosphate (CK) with elevated CK-MB isoform and/or elevated troponin)
  • Diagnostic ECG changes (e.g., >1 mm ST-segment elevation or depression in two anatomically contiguous leads)
  • Known history of CAD (i.e., past myocardial infarction, prior coronary stent Placement, and/or coronary artery bypass graft surgery)
  • Known history of thoracic aortic disease (i.e., thoracic aortic aneurysm > 5cm in diameter, history of aortic dissection, and/or history of thoracic aortic aneurysm repair (via open surgery or stent-graft placement))
  • Known history of pulmonary embolism
  • Heart rate > 100 beats per minute
  • Systolic blood pressure <105 mmHg
  • Oxygen saturation < 90%
  • Any cardiac arrhythmia causing hemodynamic compromise
  • Serum creatinine clearance <60 mL/min by Cockcroft-Gault
  • Known allergy to iodinated contrast agents
  • Subjects on metformin therapy that are unable or unwilling to discontinue therapy for 48 hours after CT procedure

Sites / Locations

  • Massachusetts General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Dedicated CT arm

Comprehensive Cardiothoracic CT arm

Arm Description

Subjects in this arm will continue to receive standard of care - that is the dedicated CT protocol to rule out either aortic dissection or acute coronary syndrome or pulmonary embolism.

The intervention consisted in a change of the routine CT protocol (as in dedicated CT protocol) to a comprehensive cardiothoracic CT protocol which includes changes in contrast injection and coverage to enable evaluation of the presence of acute coronary syndrome/aortic dissection/pulmonary embolism in a single scan.

Outcomes

Primary Outcome Measures

Length of Hospital Stay

Secondary Outcome Measures

Direct Hospital Discharge Without Imaging
Number of patients discharged without imaging
Cost of Care
Cost of stay in USD

Full Information

First Posted
February 10, 2010
Last Updated
November 27, 2017
Sponsor
Massachusetts General Hospital
Collaborators
Bracco Diagnostics, Inc
search

1. Study Identification

Unique Protocol Identification Number
NCT01067456
Brief Title
Comprehensive Cardiothoracic Dual Source CT for the Early Triage of Patients With Acute Chest Pain
Acronym
CAPTURE
Official Title
Diagnostic Value of Comprehensive Cardiothoracic Dual Source CT for the Early Triage of Patients With Undifferentiated Acute Chest Pain
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
May 2008 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
January 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
Bracco Diagnostics, Inc

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research is to determine the efficiency of a single dual source computed tomography (CT-DSCT) protocol to establish or exclude acute coronary syndrome (ACS), pulmonary embolism (PE) or aortic dissection (AD) as compared to the individual protocols. Endpoints aim to compare the rate of emergency department (ED) discharge, length of hospital stay, the diagnostic imaging test utilization, and the costs between the comprehensive and the standard protocol strategy in patients with undifferentiated chest discomfort or shortness of breath with a component of chest discomfort.
Detailed Description
Undifferentiated chest pain is one of the most common complaints in the acute care setting, accounting for over five million emergency department (ED) visits in the U.S. each year. Moreover, early and accurate triage of these patients remains difficult as neither the chest pain history, a single set of biochemical markers for myocardial necrosis, or the initial 12-lead electrocardiogram (ECG), alone or in combination, identify a group of patients that can be safely discharged without further diagnostic testing. As a result, patients presenting to the ED with undifferentiated chest pain are often evaluated with multiple examinations to exclude the presence of myocardial infarction (MI),pulmonary embolism (PE), and/or aortic dissection (AD). While contrast-enhanced spiral computed tomography angiography (CTA) has become a standard procedure in the evaluation of the presence of PE and AD, it was only within the past few years that noninvasive detection of coronary artery stenosis with CTA has become feasible. Coronary CTA has been proven to be an effective tool to rule out CAD with reported sensitivities of 93-99% and specificities of 95-97% as compared to invasive coronary angiography. Recent data from our Rule Out Myocardial Infarction by Computer Assisted Tomography (ROMICAT) study indicates that coronary CTA accurately rules out acute coronary syndrome (ACS) in patients with acute chest pain and therefore may enhance the diagnostic work up of chest pain patients in the ED. Moreover, this study demonstrated the distribution of several CT-angiographic patterns of CAD which may change management of subjects with inconclusive initial ED evaluation admitted to the hospital. For example, CTA demonstrated the absence of any CAD in 50% of the patients. None of the subjects without any CAD on CTA developed unstable angina or had an MI during index hospitalization. Furthermore, none of these patients had any MACE over the next six months, confirming previous observations in ACS patients. These data suggest that 50% of hospital admissions could be saved. Another recent study our group has demonstrated that an individually tailored ECG-gated CT protocol with a single contrast injection permits simultaneous visualization of the coronary arteries, thoracic aorta, and pulmonary arteries with excellent image quality. The very recent introduction of dual source CT (DSCT) technology offers a two-fold improvement in temporal resolution as compared to the standard 64-slice CTA that was used for these studies (83ms vs. 165ms, respectively). This significant improvement in temporal resolution allows for the acquisition of diagnostic images with higher and irregular heart rates, precluding the need for intravenous beta blockade. Given the improved temporal resolution and faster acquisition time, the amount of radiation exposure can be markedly reduced in many patients. With the need to improve triage of patients with undifferentiated chest pain and the advantages offered by DSCT technology, several observational case series have suggested the feasibility of a comprehensive thoracic DSCT (CT-DSCT) to simultaneously evaluate the coronary arteries, thoracic aorta, and pulmonary arteries. Whether this will result in an improvement of patient management and test utilization remains unclear as compared to a standard ED evaluation protocol needs to be evaluated. Thus, the purpose of this research is to determine the efficiency of a single CT-DSCT protocol to establish or exclude MI, PE, or AD as compared to the individual protocols. Endpoints aim to compare the rate of ED discharge, length of hospital stay, the diagnostic imaging test utilization, and the costs between the comprehensive and the standard protocol strategy in patients with undifferentiated chest discomfort or shortness of breath with a component of chest discomfort.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chest Pain Syndrome

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized diagnostic trial, two arms
Masking
None (Open Label)
Allocation
Randomized
Enrollment
59 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dedicated CT arm
Arm Type
No Intervention
Arm Description
Subjects in this arm will continue to receive standard of care - that is the dedicated CT protocol to rule out either aortic dissection or acute coronary syndrome or pulmonary embolism.
Arm Title
Comprehensive Cardiothoracic CT arm
Arm Type
Experimental
Arm Description
The intervention consisted in a change of the routine CT protocol (as in dedicated CT protocol) to a comprehensive cardiothoracic CT protocol which includes changes in contrast injection and coverage to enable evaluation of the presence of acute coronary syndrome/aortic dissection/pulmonary embolism in a single scan.
Intervention Type
Radiation
Intervention Name(s)
Comprehensive Cardiothoracic CT arm
Intervention Description
Subjects in this arm will receive the comprehensive cardiothoracic CT to rule out aortic dissection/pulmonary embolism/acute coronary syndrome in a single scan.
Primary Outcome Measure Information:
Title
Length of Hospital Stay
Time Frame
Index Hospitalization (within 48 hours)
Secondary Outcome Measure Information:
Title
Direct Hospital Discharge Without Imaging
Description
Number of patients discharged without imaging
Time Frame
Index Hospitalization (within 48 hours)
Title
Cost of Care
Description
Cost of stay in USD
Time Frame
Index Hospitalization (within 48 hours)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males or females >30 years of age in sinus rhythm Willing and able to provide written informed consent Undifferentiated chest discomfort or shortness of breath with a component of chest discomfort within the last 24 hours Intermediate likelihood of MI, pulmonary embolism (PE), or aortic dissection (AD) as determined by ED providers after completion of standard initial clinical evaluation ED providers independently decide that the patient's care plan should include a coronary, PE, or AD CT. Female patients must be either of non-childbearing potential (i.e., surgically sterilized or post menopausal [≥ 12 consecutive months without menses]) or must have a negative pregnancy test Exclusion Criteria: Positive cardiac biomarkers (elevated serum creatine phosphate (CK) with elevated CK-MB isoform and/or elevated troponin) Diagnostic ECG changes (e.g., >1 mm ST-segment elevation or depression in two anatomically contiguous leads) Known history of CAD (i.e., past myocardial infarction, prior coronary stent Placement, and/or coronary artery bypass graft surgery) Known history of thoracic aortic disease (i.e., thoracic aortic aneurysm > 5cm in diameter, history of aortic dissection, and/or history of thoracic aortic aneurysm repair (via open surgery or stent-graft placement)) Known history of pulmonary embolism Heart rate > 100 beats per minute Systolic blood pressure <105 mmHg Oxygen saturation < 90% Any cardiac arrhythmia causing hemodynamic compromise Serum creatinine clearance <60 mL/min by Cockcroft-Gault Known allergy to iodinated contrast agents Subjects on metformin therapy that are unable or unwilling to discontinue therapy for 48 hours after CT procedure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Udo Hoffmann, MD, MPH
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Comprehensive Cardiothoracic Dual Source CT for the Early Triage of Patients With Acute Chest Pain

We'll reach out to this number within 24 hrs