ID

42347

Beschreibung

Finding Atrial Fibrillation in Stroke - Evaluation of Enhanced and Prolonged Holter Monitoring; ODM derived from: https://clinicaltrials.gov/show/NCT01855035

Link

https://clinicaltrials.gov/show/NCT01855035

Stichworte

Versionen (1)
  1. 21.06.21 21.06.21 -
Rechteinhaber

Institut fuer anwendungsorientierte Forschung und klinische Studien GmbH

Hochgeladen am

21. Juni 2021

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0
Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Zurück zu Modell Kommentaren
Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Stroke NCT01855035

Englisch

Eligibility Stroke NCT01855035

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility Stroke NCT01855035
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
recent cerebral ischemia defined as stroke (sudden focal neurologic deficit lasting > 24h consistent with the territory of a major cerebral artery and categorised as ischemic) and/or a corresponding lesion on brain imaging.
Beschreibung

Clinical diagnosis of a stroke with or without corresponding lesion on brain imaging.

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0948008
UMLS CUI [1,2]
C0332140
UMLS CUI [1,3]
C0011923
UMLS CUI [1,4]
C1519941
UMLS CUI [1,5]
C0332185
UMLS CUI [2,1]
C0948008
UMLS CUI [2,2]
C0332140
UMLS CUI [2,3]
C0011923
UMLS CUI [2,4]
C1519941
UMLS CUI [2,5]
C0332197
UMLS CUI [2,6]
C0332185
stroke symptoms started ≤ 7 days ago.
Beschreibung

Stroke symptoms recent

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C1457887
UMLS CUI [1,3]
C0332185
age ≥ 60 years.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
modified rankin scale ≤ 2 (prior to index event).
Beschreibung

Modified rankin scale

Datentyp

boolean

Alias
UMLS CUI [1]
C2984908
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
known history of atrial fibrillation/flutter or atrial fibrillation/flutter on admission ecg.
Beschreibung

Medical history of atrial fibrillation | Medical history of flutter | Atrial fibrillation on admission ecg | Atrial flutter on admission ecg

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0004238
UMLS CUI [2,1]
C0262926
UMLS CUI [2,2]
C0004239
UMLS CUI [3,1]
C0004238
UMLS CUI [3,2]
C1623258
UMLS CUI [3,3]
C0030673
UMLS CUI [4,1]
C0004239
UMLS CUI [4,2]
C1623258
UMLS CUI [4,3]
C0030673
indication for oral anticoagulation at randomisation.
Beschreibung

Oral anticoagulation indication at randomisation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0354604
UMLS CUI [1,2]
C3146298
UMLS CUI [1,3]
C0034656
absolute contra-indication against oral anticoagulation at randomisation.
Beschreibung

Absolute contra-indication against oral anticoagulation at randomisation.

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C0205344
UMLS CUI [1,4]
C0034656
intracerebral bleeding in medical history.
Beschreibung

Medical history of intracerebral bleeding

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C2937358
patient scheduled for holter-ecg or cardiac event-recording monitoring ≥ 48 hours.
Beschreibung

Holter-ecg planned or cardiac event-recording planned

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013801
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C2825163
UMLS CUI [2,2]
C1301732
significant carotid artery or vertebral artery stenosis > 50% (nascet classification), significant intracranial artery stenosis suspicious of atherosclerotic origin or acute arterial dissection explanatory of stroke symptoms.
Beschreibung

Significant carotid artery stenosis, NASCET classification | Significant vertebral artery stenosis | Significant intracranial stenosis suspicious of atherosclerotic origin | Acute arterial dissection explanatory of stroke

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007282
UMLS CUI [1,2]
C0750502
UMLS CUI [1,3]
C3266727
UMLS CUI [2,1]
C0265103
UMLS CUI [2,2]
C0750502
UMLS CUI [3,1]
C1504438
UMLS CUI [3,2]
C0750502
UMLS CUI [3,3]
C0750493
UMLS CUI [3,4]
C2936350
UMLS CUI [4,1]
C0338585
UMLS CUI [4,2]
C0681841
UMLS CUI [4,3]
C0038454
implanted pacemaker device or cardioverter/defibrillator.
Beschreibung

Implanted pacemaker device | Implanted cardioverter/defibrillator.

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0848753
UMLS CUI [1,2]
C0150312
UMLS CUI [2,1]
C0810516
UMLS CUI [2,2]
C0150312
life expectancy < 1 year for reasons other than stroke (e.g. metastatic cancer).
Beschreibung

Life expectancy decreased for reason other than stroke

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0205216
UMLS CUI [1,3]
C0678226
UMLS CUI [1,4]
C3840932
concomitant participation in other controlled randomised trial.
Beschreibung

Concomitant participation in other controlled randomised trial.

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0008976
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Stroke NCT01855035

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility Stroke NCT01855035
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Clinical diagnosis of a stroke with or without corresponding lesion on brain imaging.
Item
recent cerebral ischemia defined as stroke (sudden focal neurologic deficit lasting > 24h consistent with the territory of a major cerebral artery and categorised as ischemic) and/or a corresponding lesion on brain imaging.
boolean
C0948008 (UMLS CUI [1,1])
C0332140 (UMLS CUI [1,2])
C0011923 (UMLS CUI [1,3])
C1519941 (UMLS CUI [1,4])
C0332185 (UMLS CUI [1,5])
C0948008 (UMLS CUI [2,1])
C0332140 (UMLS CUI [2,2])
C0011923 (UMLS CUI [2,3])
C1519941 (UMLS CUI [2,4])
C0332197 (UMLS CUI [2,5])
C0332185 (UMLS CUI [2,6])
Stroke symptoms recent
Item
stroke symptoms started ≤ 7 days ago.
boolean
C0038454 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
Age
Item
age ≥ 60 years.
boolean
C0001779 (UMLS CUI [1])
Modified rankin scale
Item
modified rankin scale ≤ 2 (prior to index event).
boolean
C2984908 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical history of atrial fibrillation | Medical history of flutter | Atrial fibrillation on admission ecg | Atrial flutter on admission ecg
Item
known history of atrial fibrillation/flutter or atrial fibrillation/flutter on admission ecg.
boolean
C0262926 (UMLS CUI [1,1])
C0004238 (UMLS CUI [1,2])
C0262926 (UMLS CUI [2,1])
C0004239 (UMLS CUI [2,2])
C0004238 (UMLS CUI [3,1])
C1623258 (UMLS CUI [3,2])
C0030673 (UMLS CUI [3,3])
C0004239 (UMLS CUI [4,1])
C1623258 (UMLS CUI [4,2])
C0030673 (UMLS CUI [4,3])
Oral anticoagulation indication at randomisation
Item
indication for oral anticoagulation at randomisation.
boolean
C0354604 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C0034656 (UMLS CUI [1,3])
Absolute contra-indication against oral anticoagulation at randomisation.
Item
absolute contra-indication against oral anticoagulation at randomisation.
boolean
C0003281 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0205344 (UMLS CUI [1,3])
C0034656 (UMLS CUI [1,4])
Medical history of intracerebral bleeding
Item
intracerebral bleeding in medical history.
boolean
C0262926 (UMLS CUI [1,1])
C2937358 (UMLS CUI [1,2])
Holter-ecg planned or cardiac event-recording planned
Item
patient scheduled for holter-ecg or cardiac event-recording monitoring ≥ 48 hours.
boolean
C0013801 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C2825163 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Significant carotid artery stenosis, NASCET classification | Significant vertebral artery stenosis | Significant intracranial stenosis suspicious of atherosclerotic origin | Acute arterial dissection explanatory of stroke
Item
significant carotid artery or vertebral artery stenosis > 50% (nascet classification), significant intracranial artery stenosis suspicious of atherosclerotic origin or acute arterial dissection explanatory of stroke symptoms.
boolean
C0007282 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C3266727 (UMLS CUI [1,3])
C0265103 (UMLS CUI [2,1])
C0750502 (UMLS CUI [2,2])
C1504438 (UMLS CUI [3,1])
C0750502 (UMLS CUI [3,2])
C0750493 (UMLS CUI [3,3])
C2936350 (UMLS CUI [3,4])
C0338585 (UMLS CUI [4,1])
C0681841 (UMLS CUI [4,2])
C0038454 (UMLS CUI [4,3])
Implanted pacemaker device | Implanted cardioverter/defibrillator.
Item
implanted pacemaker device or cardioverter/defibrillator.
boolean
C0848753 (UMLS CUI [1,1])
C0150312 (UMLS CUI [1,2])
C0810516 (UMLS CUI [2,1])
C0150312 (UMLS CUI [2,2])
Life expectancy decreased for reason other than stroke
Item
life expectancy < 1 year for reasons other than stroke (e.g. metastatic cancer).
boolean
C0023671 (UMLS CUI [1,1])
C0205216 (UMLS CUI [1,2])
C0678226 (UMLS CUI [1,3])
C3840932 (UMLS CUI [1,4])
Concomitant participation in other controlled randomised trial.
Item
concomitant participation in other controlled randomised trial.
boolean
C2348568 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
Zum Seitenanfang zurückkehren 

Kontakt

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Hilfe

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video