Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
360 participants
INTERVENTIONAL
1999-12-31
2005-01-31
Brief Summary
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Patients who come to the emergency room of Suburban Hospital in Bethesda, MD, because of chest pain may be asked to enroll in this study if they have not been diagnosed as having a heart attack. Participating patients will undergo a MRI scan as soon as emergency room doctors determine they are in stable condition. For this procedure, the patient lies on a table that slides into the MRI scanner-a large tubular machine with a magnetic field. During the scan, a contrast material is injected into the vein. This material brightens the image of the heart so that the blood flow can be seen. The scan will show if there are areas of heart muscle that received insufficient blood flow. A second scan will be done within 72 hours to look for coronary artery blockage that may require treatment. Patients will be followed by telephone 4 to 8 weeks after the scans and again 1 year after the scans to ask about any significant medical problems that may have occurred during those time periods.
This study will provide information that may improve emergency treatment of patients with acute chest pain by clarifying which patients require immediate medical treatment, which should be admitted to the hospital for further evaluation, and which may safely be discharged from the hospital.
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Detailed Description
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Conditions
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Study Design
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TREATMENT
Interventions
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MRI
Eligibility Criteria
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Inclusion Criteria
Capable of giving informed consent.
30 minutes of chest pain compatible with myocardial ischemia (chest pain score greater than 4).
Less than 270 pounds.
Exclusion Criteria
Patient states she may be pregnant (confirmed by urine or blood testing).
Severe congestive heart failure (unable to lie flat in bed).
Subjects on a mechanical ventilator.
MRI exclusions:
Subjects with a cardiac pacemaker or implantable defibrillator.
Subjects with a cerebral aneurysm clip.
Subjects with a neural stimulator (e.g. TENS-Unit).
Subjects with any type of ear implant.
Subjects with metal in eye (e.g. from machining).
Subjects with implanted devices (e.g. insulin pump, drug infusion device).
ALL
No
Sponsors
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National Heart, Lung, and Blood Institute (NHLBI)
NIH
Locations
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National Heart, Lung and Blood Institute (NHLBI)
Bethesda, Maryland, United States
Countries
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References
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Selker HP. Coronary care unit triage decision aids: how do we know when they work? Am J Med. 1989 Nov;87(5):491-3. doi: 10.1016/s0002-9343(89)80602-3. No abstract available.
Weingarten SR, Ermann B, Riedinger MS, Shah PK, Ellrodt AG. Selecting the best triage rule for patients hospitalized with chest pain. Am J Med. 1989 Nov;87(5):494-500. doi: 10.1016/s0002-9343(89)80603-5.
Tatum JL, Jesse RL, Kontos MC, Nicholson CS, Schmidt KL, Roberts CS, Ornato JP. Comprehensive strategy for the evaluation and triage of the chest pain patient. Ann Emerg Med. 1997 Jan;29(1):116-25. doi: 10.1016/s0196-0644(97)70317-2.
Other Identifiers
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00-H-0025
Identifier Type: -
Identifier Source: secondary_id
000025
Identifier Type: -
Identifier Source: org_study_id
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