Informações:
Falhas:
ID
16830
Descrição
Nesiritide Infusion for the Treatment of Decompensated Heart Failure and Renal Dysfunction; ODM derived from: https://clinicaltrials.gov/show/NCT00119691
Link
https://clinicaltrials.gov/show/NCT00119691
Palavras-chave
Versões (1)
- 09/08/2016 09/08/2016 -
Transferido a
9 de agosto de 2016
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Congestive Heart Failure NCT00119691
Eligibility Congestive Heart Failure NCT00119691
- StudyEvent: Eligibility
Similar models
Eligibility Congestive Heart Failure NCT00119691
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Decompensated cardiac failure | Hospitalization | Ventricular filling pressure increased Symptoms Quantity | Ventricular filling pressure increased Signs Quantity
Item
decompensated heart failure hospitalization with at least 1 symptom and 1 sign of elevated filling pressures
boolean
C0581377 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
C1963871 (UMLS CUI [3,1])
C1457887 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C1963871 (UMLS CUI [4,1])
C0311392 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
C0019993 (UMLS CUI [2])
C1963871 (UMLS CUI [3,1])
C1457887 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C1963871 (UMLS CUI [4,1])
C0311392 (UMLS CUI [4,2])
C1265611 (UMLS CUI [4,3])
Creatinine clearance measurement
Item
admission estimated creatinine clearance =< 50 cc/min.
boolean
C0373595 (UMLS CUI [1])
Systolic Pressure
Item
systolic blood pressure < 85 mm hg
boolean
C0871470 (UMLS CUI [1])
Shock, Cardiogenic
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
Hypovolemia
Item
volume depletion
boolean
C0546884 (UMLS CUI [1])
Myocardial Infarction | Angina, Unstable
Item
myocardial infarction, unstable angina within last 30 days
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0002965 (UMLS CUI [2])
Valvular Stenosis Significant | Hypertrophic Cardiomyopathy | Restrictive cardiomyopathy | Pericarditis, Constrictive
Item
significant valvular stenosis, hypertrophic/restrictive cardiomyopathy, or constrictive pericarditis
boolean
C1883524 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0007194 (UMLS CUI [2])
C0007196 (UMLS CUI [3])
C0031048 (UMLS CUI [4])
C0750502 (UMLS CUI [1,2])
C0007194 (UMLS CUI [2])
C0007196 (UMLS CUI [3])
C0031048 (UMLS CUI [4])
Chronic haemodialysis
Item
chronic hemodialysis
boolean
C1740835 (UMLS CUI [1])
Anticipated Major procedure During Hospitalization | Catheterization of left heart | Operative Surgical Procedures | Transplantation
Item
anticipated major procedure during hospitalization i.e. left heart catheterization, surgery, or transplantation
boolean
C0184661 (UMLS CUI [1,1])
C0205164 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,4])
C0019993 (UMLS CUI [1,5])
C0189897 (UMLS CUI [2])
C0543467 (UMLS CUI [3])
C0040732 (UMLS CUI [4])
C0205164 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,3])
C0347984 (UMLS CUI [1,4])
C0019993 (UMLS CUI [1,5])
C0189897 (UMLS CUI [2])
C0543467 (UMLS CUI [3])
C0040732 (UMLS CUI [4])
Study Subject Participation Status
Item
enrolled in another research protocol within last 30 days.
boolean
C2348568 (UMLS CUI [1])