ID

37633

Beschreibung

Anti-inflammatory Effects of Rivaroxaban Versus Dabigatran; ODM derived from: https://clinicaltrials.gov/show/NCT02331602

Link

https://clinicaltrials.gov/show/NCT02331602

Stichworte

  1. 12.08.19 12.08.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

12. August 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Atrial Fibrillation NCT02331602

Eligibility Atrial Fibrillation NCT02331602

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
non-valvular atrial fibrillation
Beschreibung

Atrial Fibrillation

Datentyp

boolean

Alias
UMLS CUI [1]
C0004238
a chads2-vasc score of 1 or more
Beschreibung

CHA2DS2-VASc score

Datentyp

boolean

Alias
UMLS CUI [1]
C4049268
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
contraindication for rivaroxaban or dabigatran
Beschreibung

Medical contraindication Rivaroxaban | Medical contraindication Dabigatran

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C1739768
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C2348066
stroke or systemic embolism, acute coronary syndromes or peripheral artery disease within 6 months before enrollment
Beschreibung

Cerebrovascular accident | EMBOLISM, SYSTEMIC ARTERIAL | Acute Coronary Syndrome | Peripheral Arterial Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0038454
UMLS CUI [2]
C0149876
UMLS CUI [3]
C0948089
UMLS CUI [4]
C1704436
acute heart failure
Beschreibung

Heart failure

Datentyp

boolean

Alias
UMLS CUI [1]
C0018801
severe chronic renal failure (creatinine clearance < 30ml/min.)
Beschreibung

Chronic Kidney Failure Severe | Creatinine clearance measurement

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0022661
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0373595
receiving dual antiplatelet therapy
Beschreibung

Antiplatelet therapy Dual

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1096021
UMLS CUI [1,2]
C0205173
patients with a body weight of 50kg or less
Beschreibung

Body Weight

Datentyp

boolean

Alias
UMLS CUI [1]
C0005910
uncontrolled hypertension
Beschreibung

Uncontrolled hypertension

Datentyp

boolean

Alias
UMLS CUI [1]
C1868885
active malignancy, collagen disease, or infectious disease
Beschreibung

Malignant Neoplasms | Collagen Disease | Communicable Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0009326
UMLS CUI [3]
C0009450
patients undergoing surgery within 6 months before enrollment
Beschreibung

Operative Surgical Procedure

Datentyp

boolean

Alias
UMLS CUI [1]
C0543467
patients who are planned to undergoing catheter ablation for atrial fibrillation
Beschreibung

Catheter ablation for atrial fibrillation Planned

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2702800
UMLS CUI [1,2]
C1301732
patients who are not allowed to participate in the trial by judgement of the treating physician
Beschreibung

Study Subject Participation Status Rejected Physician Decision

Datentyp

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548437
UMLS CUI [1,3]
C1709536

Ähnliche Modelle

Eligibility Atrial Fibrillation NCT02331602

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Atrial Fibrillation
Item
non-valvular atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
CHA2DS2-VASc score
Item
a chads2-vasc score of 1 or more
boolean
C4049268 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Rivaroxaban | Medical contraindication Dabigatran
Item
contraindication for rivaroxaban or dabigatran
boolean
C1301624 (UMLS CUI [1,1])
C1739768 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C2348066 (UMLS CUI [2,2])
Cerebrovascular accident | EMBOLISM, SYSTEMIC ARTERIAL | Acute Coronary Syndrome | Peripheral Arterial Disease
Item
stroke or systemic embolism, acute coronary syndromes or peripheral artery disease within 6 months before enrollment
boolean
C0038454 (UMLS CUI [1])
C0149876 (UMLS CUI [2])
C0948089 (UMLS CUI [3])
C1704436 (UMLS CUI [4])
Heart failure
Item
acute heart failure
boolean
C0018801 (UMLS CUI [1])
Chronic Kidney Failure Severe | Creatinine clearance measurement
Item
severe chronic renal failure (creatinine clearance < 30ml/min.)
boolean
C0022661 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0373595 (UMLS CUI [2])
Antiplatelet therapy Dual
Item
receiving dual antiplatelet therapy
boolean
C1096021 (UMLS CUI [1,1])
C0205173 (UMLS CUI [1,2])
Body Weight
Item
patients with a body weight of 50kg or less
boolean
C0005910 (UMLS CUI [1])
Uncontrolled hypertension
Item
uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1])
Malignant Neoplasms | Collagen Disease | Communicable Disease
Item
active malignancy, collagen disease, or infectious disease
boolean
C0006826 (UMLS CUI [1])
C0009326 (UMLS CUI [2])
C0009450 (UMLS CUI [3])
Operative Surgical Procedure
Item
patients undergoing surgery within 6 months before enrollment
boolean
C0543467 (UMLS CUI [1])
Catheter ablation for atrial fibrillation Planned
Item
patients who are planned to undergoing catheter ablation for atrial fibrillation
boolean
C2702800 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Study Subject Participation Status Rejected Physician Decision
Item
patients who are not allowed to participate in the trial by judgement of the treating physician
boolean
C2348568 (UMLS CUI [1,1])
C1548437 (UMLS CUI [1,2])
C1709536 (UMLS CUI [1,3])

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