ID

23047

Description

Renal Effects of Levosimendan in Patients Admitted With Acute Decompensated Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00527059

Lien

https://clinicaltrials.gov/show/NCT00527059

Mots-clés

  1. 21/06/2017 21/06/2017 -
Téléchargé le

21 juin 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Heart Failure NCT00527059

Eligibility Heart Failure NCT00527059

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
an ejection fraction (ef) 40% by transthoracic echocardiogram,
Description

ID.1

Type de données

boolean

Alias
UMLS CUI [1]
C2700378
a baseline pulmonary capillary wedge pressure (pcwp) 20 mm hg
Description

ID.2

Type de données

boolean

Alias
UMLS CUI [1]
C0086879
a mdrd (modification of diet renal disease) score > 30 and < 60
Description

ID.3

Type de données

boolean

Alias
UMLS CUI [1]
C1980036
and a standard therapy for hf that should include angiotensin converting enzyme inhibitors, angiotensin receptor blockers, aldosterone blocking agents (spironolactone) and beta-blockers, unless contraindicated
Description

ID.4

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0087111
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients receiving other oral or i.v. inotropes,
Description

ID.5

Type de données

boolean

Alias
UMLS CUI [1]
C0304509
oral or i.v. diuretics
Description

ID.6

Type de données

boolean

Alias
UMLS CUI [1]
C0012798
or receiving nitroglycerine or nitroprusside,
Description

ID.7

Type de données

boolean

Alias
UMLS CUI [1,1]
C0017887
UMLS CUI [1,2]
C0028193
patients with systolic blood pressure <110 mmhg,
Description

ID.8

Type de données

boolean

Alias
UMLS CUI [1]
C0277885
mechanical ventilation,
Description

ID.9

Type de données

boolean

Alias
UMLS CUI [1]
C0199470
anticipated survival <30 days,
Description

ID.10

Type de données

boolean

Alias
UMLS CUI [1]
C0038952
absence of thoracic windows for echocardiography,
Description

ID.11

Type de données

boolean

Alias
UMLS CUI [1]
C0013516
acute coronary syndromes,
Description

ID.12

Type de données

boolean

Alias
UMLS CUI [1]
C0948089
sustained ventricular tachycardia or ventricular fibrillation,
Description

ID.13

Type de données

boolean

Alias
UMLS CUI [1,1]
C0042514
UMLS CUI [1,2]
C0042510
documented renal artery stenosis, requiring dialysis,
Description

ID.14

Type de données

boolean

Alias
UMLS CUI [1,1]
C0035067
UMLS CUI [1,2]
C0011945
requiring admission primarily for concurrent morbidity,
Description

ID.15

Type de données

boolean

Alias
UMLS CUI [1]
C0012634
severe aortic or mitral regurgitation,
Description

ID.16

Type de données

boolean

Alias
UMLS CUI [1,1]
C0026266
UMLS CUI [1,2]
C0003504
left ventricular failure primarily from uncorrected obstructive valvular disease, hypertrophic obstructive cardiomyopathy, restrictive/obstructive cardiomyopathy,
Description

ID.17

Type de données

boolean

Alias
UMLS CUI [1]
C0849925
uncorrected thyroid disease,
Description

ID.18

Type de données

boolean

Alias
UMLS CUI [1]
C0040128
known amyloid cardiomyopathy
Description

ID.19

Type de données

boolean

Alias
UMLS CUI [1]
C1387310
or known malfunctioning artificial heart valve.
Description

ID.20

Type de données

boolean

Alias
UMLS CUI [1,1]
C0444231
UMLS CUI [1,2]
C1394026

Similar models

Eligibility Heart Failure NCT00527059

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
an ejection fraction (ef) 40% by transthoracic echocardiogram,
boolean
C2700378 (UMLS CUI [1])
ID.2
Item
a baseline pulmonary capillary wedge pressure (pcwp) 20 mm hg
boolean
C0086879 (UMLS CUI [1])
ID.3
Item
a mdrd (modification of diet renal disease) score > 30 and < 60
boolean
C1980036 (UMLS CUI [1])
ID.4
Item
and a standard therapy for hf that should include angiotensin converting enzyme inhibitors, angiotensin receptor blockers, aldosterone blocking agents (spironolactone) and beta-blockers, unless contraindicated
boolean
C0018801 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
ID.5
Item
patients receiving other oral or i.v. inotropes,
boolean
C0304509 (UMLS CUI [1])
ID.6
Item
oral or i.v. diuretics
boolean
C0012798 (UMLS CUI [1])
ID.7
Item
or receiving nitroglycerine or nitroprusside,
boolean
C0017887 (UMLS CUI [1,1])
C0028193 (UMLS CUI [1,2])
ID.8
Item
patients with systolic blood pressure <110 mmhg,
boolean
C0277885 (UMLS CUI [1])
ID.9
Item
mechanical ventilation,
boolean
C0199470 (UMLS CUI [1])
ID.10
Item
anticipated survival <30 days,
boolean
C0038952 (UMLS CUI [1])
ID.11
Item
absence of thoracic windows for echocardiography,
boolean
C0013516 (UMLS CUI [1])
ID.12
Item
acute coronary syndromes,
boolean
C0948089 (UMLS CUI [1])
ID.13
Item
sustained ventricular tachycardia or ventricular fibrillation,
boolean
C0042514 (UMLS CUI [1,1])
C0042510 (UMLS CUI [1,2])
ID.14
Item
documented renal artery stenosis, requiring dialysis,
boolean
C0035067 (UMLS CUI [1,1])
C0011945 (UMLS CUI [1,2])
ID.15
Item
requiring admission primarily for concurrent morbidity,
boolean
C0012634 (UMLS CUI [1])
ID.16
Item
severe aortic or mitral regurgitation,
boolean
C0026266 (UMLS CUI [1,1])
C0003504 (UMLS CUI [1,2])
ID.17
Item
left ventricular failure primarily from uncorrected obstructive valvular disease, hypertrophic obstructive cardiomyopathy, restrictive/obstructive cardiomyopathy,
boolean
C0849925 (UMLS CUI [1])
ID.18
Item
uncorrected thyroid disease,
boolean
C0040128 (UMLS CUI [1])
ID.19
Item
known amyloid cardiomyopathy
boolean
C1387310 (UMLS CUI [1])
ID.20
Item
or known malfunctioning artificial heart valve.
boolean
C0444231 (UMLS CUI [1,1])
C1394026 (UMLS CUI [1,2])

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