- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02137980
Registry of Non-primary Angioplasty at Hospitals Without Surgery On-site (CPORT)
10. april 2018 opdateret af: Johns Hopkins University
This is a simple registry of patients undergoing PCI at hospitals without surgery on-site who were participants in the CPORT-E project.
The aim of the registry is simple data collection and reporting to respective State Departments of Health.
The registry population consists of patients undergoing diagnostic cardiac catheterization for suspected CAD at hospitals without SOS and who require PCI.
Studieoversigt
Status
Afsluttet
Betingelser
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
31390
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Alabama
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Huntsville, Alabama, Forenede Stater, 35801
- Crestwood Medical Center
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Maryland
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Annapolis, Maryland, Forenede Stater, 21401
- Anne Arundel Medical Center
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Baltimore, Maryland, Forenede Stater, 21044
- Hopkins Bayview Medical Center
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Catonsville, Maryland, Forenede Stater, 21229
- St. Agnes Hospital
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Clinton, Maryland, Forenede Stater, 20735
- Southern Maryland Hospital Center
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Frederick, Maryland, Forenede Stater, 21701
- Frederick Memorial Hospital
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Glen Burnie, Maryland, Forenede Stater, 21061
- Baltimore Washington Medical Center
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Hagerstown, Maryland, Forenede Stater, 21742
- Meritus Medical Center
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Rockville, Maryland, Forenede Stater, 20850
- Shady Grove Adventist Hospital
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New Jersey
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Bayonne, New Jersey, Forenede Stater, 07002
- Bayonne Medical Center
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Belleville, New Jersey, Forenede Stater, 07109
- Clara Maas Medical Center
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Edison, New Jersey, Forenede Stater, 08818
- JFK Medical Center
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Elizabeth, New Jersey, Forenede Stater, 07207
- Trinitas Hospital
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Marlton, New Jersey, Forenede Stater, 08053
- Virtua West Jersey Hospital
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Perth Amboy, New Jersey, Forenede Stater, 08861
- Raritan Bay Medical Center
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Red Bank, New Jersey, Forenede Stater, 07701
- Riverview Medical Center
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Somerville, New Jersey, Forenede Stater, 08876
- Somerset Medical Center
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Summit, New Jersey, Forenede Stater, 07901
- Overlook Hospital
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Teaneck, New Jersey, Forenede Stater, 07666
- Holy Name Hospital
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Toms River, New Jersey, Forenede Stater, 08755
- Community Medical Center
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Ohio
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Bryan, Ohio, Forenede Stater, 43506
- Community Health and Wellness Center
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Chardon, Ohio, Forenede Stater, 44024
- University Hospital Geauga Medical Center
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Columbus, Ohio, Forenede Stater, 43205
- Ohio State University Hospital East
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Columbus, Ohio, Forenede Stater, 43213
- Mt. Carmel St. Ann Hospital
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Dayton, Ohio, Forenede Stater, 45459
- Southview Medical Center
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Hamilton, Ohio, Forenede Stater, 45013
- Fort Hamilton Hospital
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Marietta, Ohio, Forenede Stater, 45750
- Marietta Memorial Hospital
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Mount Vernon, Ohio, Forenede Stater, 43050
- Knox Community Hospital
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Newark, Ohio, Forenede Stater, 43055
- Licking Memorial Hospital
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West Chester, Ohio, Forenede Stater, 45069
- West Chester Hospital
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Pennsylvania
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Kittanning, Pennsylvania, Forenede Stater, 16201
- Armstrong County Memorial Hospital
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Lewisburg, Pennsylvania, Forenede Stater, 17837
- Evangelical Community Hospital
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McKeesport, Pennsylvania, Forenede Stater, 15132
- UPMC McKeesport
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Meadville, Pennsylvania, Forenede Stater, 16335
- Meadville Medical Center
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Monongahela, Pennsylvania, Forenede Stater, 15063
- Monongahela Valley Hospital
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Philadelphia, Pennsylvania, Forenede Stater, 19152
- Nazareth Hospital
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York, Pennsylvania, Forenede Stater, 17403
- Memorial Hospital
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 95 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
The patient population includes inpatients and outpatients undergoing diagnostic cardiac catheterization for suspected coronary artery disease (CAD) at hospitals without SOS.
Beskrivelse
Inclusion Criteria:
Patient inclusion criteria are:
Pre-catheterization
- must be undergoing diagnostic cardiac catheterization for suspected CAD
- be at least 18 years of age
- must not be pregnant (negative pregnancy test) or must not be of childbearing potential
- must be able to give informed consent. Post-catheterization
- coronary artery disease judged to be clinically and angiographically significant
- ability to perform PCI with equipment available at the local site (see below)
- procedure risk judged to be not high (see below)
Exclusion Criteria:
Patient exclusion criteria are:
Pre-catheterization
- inability to give informed consent
- ST-segment elevation myocardial infarction
- pregnancy Post-catheterization
- high likelihood of requiring a device not available at the hospitals without SOS (see below)
- no need for PCI
- need for coronary artery bypass surgery
- high procedural risk (see below)
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Number of participants with adverse events
Tidsramme: Thru Index or Transfer Hospital Discharge on average 24 hours
|
Thru Index or Transfer Hospital Discharge on average 24 hours
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: Thomas Aversano, MD, Johns Hopkins University
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. april 2011
Primær færdiggørelse (Faktiske)
31. december 2015
Studieafslutning (Faktiske)
1. marts 2016
Datoer for studieregistrering
Først indsendt
18. marts 2014
Først indsendt, der opfyldte QC-kriterier
13. maj 2014
Først opslået (Skøn)
14. maj 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
12. april 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
10. april 2018
Sidst verificeret
1. april 2018
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- NA_00046362
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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