- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01035047
Randomiseret undersøgelse af brystsmertediagnostiske strategier
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
På trods af at de årligt bruger 12 milliarder dollars på nødevaluering af brystsmerter i USA, har kun 15 % af indlagte patienter en hjerteårsag til deres symptomer. Kliniske beslutningsenheder (CDU'er) forbedrer ressourceudnyttelsen og er en anbefalet behandlingsmulighed af American College of Cardiology/American Heart Association, men er underudnyttet hos ikke-lavrisiko brystsmertepatienter på grund af svagheder ved traditionelle hjertetests. Cardiac magnetic resonance imaging (CMR) er følsom og specifik for iskæmi, kan samtidig vurdere hjertefunktion og myokardieperfusion og kan revolutionere den diagnostiske proces for patienter med mellemrisiko og brystsmerter. Den overlegne nøjagtighed af CMR kan reducere testning og invasive procedurer. Den høje følsomhed for igangværende iskæmi kunne tillade billeddannelse parallelt med hjertemarkører. Som et resultat heraf kunne CMR forbedre plejen af akutmodtagelsespatienter (ED) med brystsmerter med mellemrisiko. Effektiviteten og sikkerheden af CMR er dog ikke blevet grundigt testet i CDU-indstillingen.
Primær hypotese: En CDU-CMR-strategi vil reducere forekomsten af sammensætningen af revaskularisering, re-hospitalisering og tilbagevendende hjertetest efter 90 dage sammenlignet med en indlæggelsesstrategi.
Metoder: Deltagere (n=146) med mellemrisiko for akut koronarsyndrom (ACS) vil blive rekrutteret til et klinisk forsøg fra Wake Forest University Baptist Medical Center (WFUBMC) ED. Deltagerne vil ligeligt blive randomiseret til CDU-CMR eller indlæggelse. CDU-CMR deltagere vil gennemgå hvile og stress CMR billeddannelse parallelt med serielle hjertemarkører. Indlæggelsesdeltagere vil gennemgå serielle hjertemarkører efterfulgt af eksisterende hjertetests som bestemt af deres behandlere. Det primære resultat er sammensætningen af 90 dages revaskularisering, genindlæggelse og tilbagevendende hjertetest. Det sekundære resultat er indeks indlæggelseslængde på liggetid. Sikkerhedshændelser omfatter ACS efter udskrivelse, dødelighed og stresstest-relaterede bivirkninger.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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North Carolina
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Winston-Salem, North Carolina, Forenede Stater, 27157
- Wake Forest University Baptist Medical Center
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inklusionskriterier:
- Alder over eller lig med 21 år på tilmeldingstidspunktet
- Ubehag i brystet eller andre symptomer i overensstemmelse med mulig ACS som angivet af den behandlende læge efter opnåelse af et EKG og hjertebiomarkører til patientens evaluering
- Trombolyse ved myokardieinfarkt (TIMI) risikoscore >/= 2 eller lægens indtryk af intermediære eller høje sandsynlige symptomer repræsenterer ACS
- Patienten kræver en indlæggelses- eller CDU-evaluering for deres brystsmerter
- Den behandlende læge mener, at patienten kunne blive udskrevet hjem, hvis hjertesygdom blev udelukket
- Den behandlende læge føler, at patienten er sikker for CDU-behandling
Prætest-sandsynlighedsvurdering Vurderingen af mellemliggende risiko for udvikling af ACS vil være baseret på en TIMI-risikoscore >/= 2 og/eller en bestyrelsescertificeret/bestyrelseskvalificeret akutlæge klinisk indtryk af mellemliggende eller høj sandsynlighed for, at symptomerne repræsenterer ACS. Læger opfordres til at bruge 2007 American College of Cardiology (ACC)/American Heart Association (AHA) retningslinjer som en ramme for denne vurdering.
Ekskluderingskriterier:
- Forhøjede hjertebiomarkører
- Ny ST-segment elevation på ethvert elektrokardiogram (>/= 1 mV)
- Ny ST-segment depression på ethvert elektrokardiogram (>/= 2 mV)
- Kendt inducerbar hjerteiskæmi uden efterfølgende revaskularisering
- Ude af stand til at ligge fladt
- Symptomatisk hypotension på tidspunktet for indskrivning (systolisk < 90 mm Hg)
- Kontraindikationer til MR (eksempler: pacemaker, defibrillator, cerebral aneurisme clips, metallisk okulært fremmedlegeme, implanteret udstyr, svær klaustrofobi)
- Patient afslag på eller manglende evne til at overholde journalgennemgang og opfølgning
- Terminaldiagnose med forventet levetid mindre end 3 måneder
- I øjeblikket gravid
- Kreatininclearance < 45 ml/min på tidspunktet for indskrivning eller klinisk bekymring for akut nyreskade
- Kronisk leversygdom med en kreatininclearance på <60 ml/min på indskrivningstidspunktet
- Hepato-renalt syndrom
- Historie om lever-, hjerte- eller nyretransplantation
- Bekræftet angioplastik, stentplacering eller koronararterie bypass grafting (CABG) inden for de sidste 6 måneder
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Diagnostisk
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Ingen indgriben: Indlæggelse
Dette er sammenligningsarmen.
Patienterne bliver indlagt på hospitalet og gennemgår sædvanlig pleje.
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Eksperimentel: CDU-CMR protokol
Patienterne vil blive overført til den kliniske beslutningsenhed og gennemgå en stress-hjerte-MR-evaluering.
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Efter ED-evaluering randomiseres patienterne til klinisk beslutningsenhedspleje eller indlæggelse.
Patienter i den kliniske beslutningsenhed vil også gennemgå en stress-hjerte-MR.
Patienter i den indlagte plejearm kan gennemgå enhver ønsket test, herunder hjerte-MRI, som bestemt af deres behandlende læge.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
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Sammensætningen af revaskularisering, re-hospitalisering og tilbagevendende hjertetest gennem 90 dage.
Tidsramme: Indeks Hospitalsindlæggelse gennem 90 dage
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Indeks Hospitalsindlæggelse gennem 90 dage
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Sekundære resultatmål
Resultatmål |
Tidsramme |
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Opholdsvarighed
Tidsramme: Varighed af Indeks Hospitalsindlæggelse, i gennemsnit 1-2 dage
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Varighed af Indeks Hospitalsindlæggelse, i gennemsnit 1-2 dage
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Akut koronarsyndrom
Tidsramme: Indeks Indlæggelsesudskrivning gennem 90 dage
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Indeks Indlæggelsesudskrivning gennem 90 dage
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Dødelighed
Tidsramme: Indeks Hospitalsindlæggelse gennem 90 dage
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Indeks Hospitalsindlæggelse gennem 90 dage
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Stresstest-relateret bivirkning
Tidsramme: Indeks Hospitalsindlæggelse gennem 90 dage
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Indeks Hospitalsindlæggelse gennem 90 dage
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Samarbejdspartnere og efterforskere
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Chadwick Miller, M.D., WFUBMC
Publikationer og nyttige links
Generelle publikationer
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- Myocardial infarction redefined--a consensus document of The Joint European Society of Cardiology/American College of Cardiology Committee for the redefinition of myocardial infarction. Eur Heart J. 2000 Sep;21(18):1502-13. doi: 10.1053/euhj.2000.2305.
- Farkouh ME, Smars PA, Reeder GS, Zinsmeister AR, Evans RW, Meloy TD, Kopecky SL, Allen M, Allison TG, Gibbons RJ, Gabriel SE. A clinical trial of a chest-pain observation unit for patients with unstable angina. Chest Pain Evaluation in the Emergency Room (CHEER) Investigators. N Engl J Med. 1998 Dec 24;339(26):1882-8. doi: 10.1056/NEJM199812243392603.
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- Patel MR, Dehmer GJ, Hirshfeld JW, Smith PK, Spertus JA; American College of Cardiology Foundation Appropriateness Criteria Task Force; Society for Cardiovascular Angiography and Interventions; Society of Thoracic Surgeons; American Association for Thoracic Surgery; American Heart Association, and the American Society of Nuclear Cardiology Endorsed by the American Society of Echocardiography; Heart Failure Society of America; Society of Cardiovascular Computed Tomography. ACCF/SCAI/STS/AATS/AHA/ASNC 2009 Appropriateness Criteria for Coronary Revascularization: a report by the American College of Cardiology Foundation Appropriateness Criteria Task Force, Society for Cardiovascular Angiography and Interventions, Society of Thoracic Surgeons, American Association for Thoracic Surgery, American Heart Association, and the American Society of Nuclear Cardiology Endorsed by the American Society of Echocardiography, the Heart Failure Society of America, and the Society of Cardiovascular Computed Tomography. J Am Coll Cardiol. 2009 Feb 10;53(6):530-53. doi: 10.1016/j.jacc.2008.10.005.
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- Smith SC Jr, Feldman TE, Hirshfeld JW Jr, Jacobs AK, Kern MJ, King SB 3rd, Morrison DA, O'Neill WW, Schaff HV, Whitlow PL, Williams DO, Antman EM, Smith SC Jr, Adams CD, Anderson JL, Faxon DP, Fuster V, Halperin JL, Hiratzka LF, Hunt SA, Jacobs AK, Nishimura R, Ornato JP, Page RL, Riegel B; American College of Cardiology/American Heart Association Task Force on Practice Guidelines; ACC/AHA/SCAI Writing Committee to Update the 2001 Guidelines for Percutaneous Coronary Intervention. ACC/AHA/SCAI 2005 guideline update for percutaneous coronary intervention: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (ACC/AHA/SCAI Writing Committee to Update the 2001 Guidelines for Percutaneous Coronary Intervention). J Am Coll Cardiol. 2006 Jan 3;47(1):e1-121. doi: 10.1016/j.jacc.2005.12.001. No abstract available.
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- Ferreira-Gonzalez I, Permanyer-Miralda G, Busse JW, Bryant DM, Montori VM, Alonso-Coello P, Walter SD, Guyatt GH. Methodologic discussions for using and interpreting composite endpoints are limited, but still identify major concerns. J Clin Epidemiol. 2007 Jul;60(7):651-7; discussion 658-62. doi: 10.1016/j.jclinepi.2006.10.020. Epub 2007 Feb 23.
- Tsushima Y, Aoki J, Endo K. Contribution of the diagnostic test to the physician's diagnostic thinking: new method to evaluate the effect. Acad Radiol. 2003 Jul;10(7):751-5. doi: 10.1016/s1076-6332(03)80120-4.
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- Miller CD, Case LD, Little WC, Mahler SA, Burke GL, Harper EN, Lefebvre C, Hiestand B, Hoekstra JW, Hamilton CA, Hundley WG. Stress CMR reduces revascularization, hospital readmission, and recurrent cardiac testing in intermediate-risk patients with acute chest pain. JACC Cardiovasc Imaging. 2013 Jul;6(7):785-94. doi: 10.1016/j.jcmg.2012.11.022. Epub 2013 May 8.
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Andre undersøgelses-id-numre
- IRB00010410
- 1R21HL097131-01A1 (U.S. NIH-bevilling/kontrakt)
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
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