ID

20835

Description

RED-HF™ Trial - Reduction of Events With Darbepoetin Alfa in Heart Failure Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00358215

Lien

https://clinicaltrials.gov/show/NCT00358215

Mots-clés

  1. 21/03/2017 21/03/2017 -
Téléchargé le

21 mars 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Heart Failure NCT00358215

Eligibility Heart Failure NCT00358215

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
heart failure of at least 3 months duration and of new york heart association (nyha) class ii, iii, or iv
Description

Heart failure Duration New York Heart Association Classification

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0449238
UMLS CUI [1,3]
C1275491
hemoglobin between 9.0 g/dl and 12.0 g/dl
Description

Hemoglobin measurement

Type de données

boolean

Alias
UMLS CUI [1]
C0518015
left ventricular ejection fraction equal to or less than 40%
Description

Left ventricular ejection fraction

Type de données

boolean

Alias
UMLS CUI [1]
C0428772
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
transferrin saturation (tsat) < 15%
Description

Transferrin saturation measurement

Type de données

boolean

Alias
UMLS CUI [1]
C1277709
blood pressure > 160/100 mm hg
Description

Blood Pressure

Type de données

boolean

Alias
UMLS CUI [1]
C0005823
heart failure primarily due to valvular heart disease or clinically significant valvular heart disease that might lead to surgical correction within 12 months of randomization
Description

Heart failure Due to Heart valve disease | Heart valve disease Causing Correction Surgical

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0018824
UMLS CUI [2,1]
C0018824
UMLS CUI [2,2]
C0678227
UMLS CUI [2,3]
C1947976
UMLS CUI [2,4]
C0543467
recipient of a major organ transplant or receiving renal replacement therapy
Description

Transplant Recipient Organ Major | Renal Replacement Therapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0376387
UMLS CUI [1,2]
C0178784
UMLS CUI [1,3]
C0205164
UMLS CUI [2]
C0206074
serum creatinine > 3.0 mg/dl (> 265 µmol/l)
Description

Creatinine measurement, serum

Type de données

boolean

Alias
UMLS CUI [1]
C0201976

Similar models

Eligibility Heart Failure NCT00358215

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Heart failure Duration New York Heart Association Classification
Item
heart failure of at least 3 months duration and of new york heart association (nyha) class ii, iii, or iv
boolean
C0018801 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
Hemoglobin measurement
Item
hemoglobin between 9.0 g/dl and 12.0 g/dl
boolean
C0518015 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction equal to or less than 40%
boolean
C0428772 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Transferrin saturation measurement
Item
transferrin saturation (tsat) < 15%
boolean
C1277709 (UMLS CUI [1])
Blood Pressure
Item
blood pressure > 160/100 mm hg
boolean
C0005823 (UMLS CUI [1])
Heart failure Due to Heart valve disease | Heart valve disease Causing Correction Surgical
Item
heart failure primarily due to valvular heart disease or clinically significant valvular heart disease that might lead to surgical correction within 12 months of randomization
boolean
C0018801 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0018824 (UMLS CUI [1,3])
C0018824 (UMLS CUI [2,1])
C0678227 (UMLS CUI [2,2])
C1947976 (UMLS CUI [2,3])
C0543467 (UMLS CUI [2,4])
Transplant Recipient Organ Major | Renal Replacement Therapy
Item
recipient of a major organ transplant or receiving renal replacement therapy
boolean
C0376387 (UMLS CUI [1,1])
C0178784 (UMLS CUI [1,2])
C0205164 (UMLS CUI [1,3])
C0206074 (UMLS CUI [2])
Creatinine measurement, serum
Item
serum creatinine > 3.0 mg/dl (> 265 µmol/l)
boolean
C0201976 (UMLS CUI [1])

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