ID

12598

Beschrijving

BAY58-2667 Dose Finding Trial Investigating Fixed Doses in Patients With Acute Decompensated Chronic Congestive Heart Failure (ADHF); ODM derived from: https://clinicaltrials.gov/show/NCT01065077

Link

https://clinicaltrials.gov/show/NCT01065077

Trefwoorden

  1. 04-12-15 04-12-15 -
Geüploaded op

4 december 2015

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Acute Heart Failure NCT01065077

Eligibility Acute Heart Failure NCT01065077

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female subjects, age >/= 18 years of age
Beschrijving

non-pregnant, non-lactating or women without childbearing potential

Datatype

boolean

Alias
UMLS CUI [1]
C0150831
UMLS CUI [2]
C0001779
Postmenopausal women aged 18 years or older.
Beschrijving

Postmenopausal women

Datatype

boolean

Alias
UMLS CUI [1]
C0232970
women with bilateral tubal ligation, women with bilateral ovariectomy, and women with a hysterectomy
Beschrijving

adequate contraceptive methods

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
subjects must have the clinical diagnosis of chf made at least three months prior to enrollment
Beschrijving

congestive heart failure diagnosis

Datatype

boolean

Alias
UMLS CUI [1]
C0018802
subjects must experience worsening of both of the symptoms below leading to hospitalization at the time of entry into the study:
Beschrijving

subjects must experience worsening of both of the symptoms below leading to hospitalization

Datatype

boolean

Alias
UMLS CUI [1]
C1821820
UMLS CUI [2]
C0019993
dyspnea
Beschrijving

dyspnea

Datatype

boolean

Alias
UMLS CUI [1]
C0013404
clinical evidence of volume overload
Beschrijving

volume overload

Datatype

boolean

Alias
UMLS CUI [1]
C2236137
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
Pregnancy or breastfeeding
Beschrijving

Pregnancy or breastfeeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
acute de-novo heart failure
Beschrijving

acute new heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0742752
acute myocardial infarction and/or myocardial infarction within 30 days
Beschrijving

acute myocardial infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0155626
valvular heart disease requiring surgical intervention during the course of the study
Beschrijving

valvular heart disease

Datatype

boolean

Alias
UMLS CUI [1]
C0018824
heart failure due to or associated with uncorrected primary valvular disease, malfunctioning artificial heart valve, or uncorrected congenital heart disease
Beschrijving

heart failure due to or associated with uncorrected primary valvular disease, malfunctioning artificial heart valve, or uncorrected congenital heart disease

Datatype

boolean

Alias
UMLS CUI [1]
C0018801
UMLS CUI [2]
C0018824
UMLS CUI [3]
C0152021
primary hypertrophic cardiomyopathy
Beschrijving

primary hypertrophic cardiomyopathy

Datatype

boolean

Alias
UMLS CUI [1]
C0264847
acute inflammatory heart disease,eg, acute myocarditis
Beschrijving

acute inflammatory heart disease,eg, acute myocarditis

Datatype

boolean

Alias
UMLS CUI [1]
C0027059
UMLS CUI [2]
C0014118
UMLS CUI [3]
C0031046
unstable angina requiring angiography
Beschrijving

unstable angina

Datatype

boolean

Alias
UMLS CUI [1]
C0002965

Similar models

Eligibility Acute Heart Failure NCT01065077

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Patient age and sex
Item
male and female subjects, age >/= 18 years of age
boolean
C0150831 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Postmenopausal women
Item
Postmenopausal women aged 18 years or older.
boolean
C0232970 (UMLS CUI [1])
adequate contraceptive methods
Item
women with bilateral tubal ligation, women with bilateral ovariectomy, and women with a hysterectomy
boolean
C0700589 (UMLS CUI [1])
congestive heart failure diagnosis
Item
subjects must have the clinical diagnosis of chf made at least three months prior to enrollment
boolean
C0018802 (UMLS CUI [1])
subjects must experience worsening of both of the symptoms below leading to hospitalization
Item
subjects must experience worsening of both of the symptoms below leading to hospitalization at the time of entry into the study:
boolean
C1821820 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
dyspnea
Item
dyspnea
boolean
C0013404 (UMLS CUI [1])
volume overload
Item
clinical evidence of volume overload
boolean
C2236137 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy or breastfeeding
Item
Pregnancy or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
acute new heart failure
Item
acute de-novo heart failure
boolean
C0742752 (UMLS CUI [1])
acute myocardial infarction
Item
acute myocardial infarction and/or myocardial infarction within 30 days
boolean
C0155626 (UMLS CUI [1])
valvular heart disease
Item
valvular heart disease requiring surgical intervention during the course of the study
boolean
C0018824 (UMLS CUI [1])
heart failure due to or associated with uncorrected primary valvular disease, malfunctioning artificial heart valve, or uncorrected congenital heart disease
Item
heart failure due to or associated with uncorrected primary valvular disease, malfunctioning artificial heart valve, or uncorrected congenital heart disease
boolean
C0018801 (UMLS CUI [1])
C0018824 (UMLS CUI [2])
C0152021 (UMLS CUI [3])
primary hypertrophic cardiomyopathy
Item
primary hypertrophic cardiomyopathy
boolean
C0264847 (UMLS CUI [1])
acute inflammatory heart disease,eg, acute myocarditis
Item
acute inflammatory heart disease,eg, acute myocarditis
boolean
C0027059 (UMLS CUI [1])
C0014118 (UMLS CUI [2])
C0031046 (UMLS CUI [3])
unstable angina
Item
unstable angina requiring angiography
boolean
C0002965 (UMLS CUI [1])

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