Informations:
Erreur:
ID
12608
Description
A Study to Evaluate the Efficacy and Safety of Shenfu Zhusheye in Patients With Acute Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT02135835
Lien
https://clinicaltrials.gov/show/NCT02135835
Mots-clés
Versions (1)
- 04/12/2015 04/12/2015 -
Téléchargé le
4 décembre 2015
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
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Eligibility Acute Heart Failure NCT02135835
Eligibility Acute Heart Failure NCT02135835
- StudyEvent: Eligibility
Similar models
Eligibility Acute Heart Failure NCT02135835
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
acute heart failure
Item
clinical diagnosis of acute heart failure according to guidelines for the diagnosis and treatment of acute heart failure 2010 of chinese medical association(participants whose heart function grade of nyha is ).
boolean
C0264714 (UMLS CUI [1])
lvef
Item
lvef≤40%.
boolean
C0428772 (UMLS CUI [1])
nt-pro-bnp ≥1400 pg/ml or bnp ≥ 350pg/ml
Item
nt-pro-bnp ≥1400 pg/ml or bnp ≥ 350pg/ml.
boolean
C1095989 (UMLS CUI [1])
C3272900 (UMLS CUI [2])
C3272900 (UMLS CUI [2])
patient age and sex
Item
ages 18-80, male or female.
boolean
C0150831 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
informed consent
Item
all participants signed the informed consent.
boolean
C0021430 (UMLS CUI [1])
liver dysfunction
Item
participants with abnormal liver function (alt, ast≥3 times of upper limit of normal) or abnormal kidney function( cr≥1.5 times of upper limit of normal or cr >3.0 mg/dl (> 265 µmol/l)).
boolean
C0086565 (UMLS CUI [1])
systolic blood pressure
Item
sbp ≥ 150mmhg.
boolean
C0871470 (UMLS CUI [1])
participants with severe chronic asthmatic bronchitis or acute episode of lung diseases
Item
participants with severe chronic asthmatic bronchitis or acute episode of lung diseases.
boolean
C0264348 (UMLS CUI [1])
C0024115 (UMLS CUI [2])
C0024115 (UMLS CUI [2])
participants with acute coronary syndrome, cardiogenic shock, aortic dissection, pulmonary embolism, severe ventricular arrhythmias, complete atrioventricular block without cardiac pacemaker, hypertrophic obstructive cardiomyopathy, restrictive cardiomyopathy and severe valvular disease without surgery
Item
participants with acute coronary syndrome, cardiogenic shock, aortic dissection, pulmonary embolism, severe ventricular arrhythmias, complete atrioventricular block without cardiac pacemaker, hypertrophic obstructive cardiomyopathy, restrictive cardiomyopathy and severe valvular disease without surgery.
boolean
C0948089 (UMLS CUI [1])
C0036980 (UMLS CUI [2])
C0878544 (UMLS CUI [3])
C0036980 (UMLS CUI [2])
C0878544 (UMLS CUI [3])
participants with advanced cancer.
Item
participants with advanced cancer.
boolean
C0006826 (UMLS CUI [1])
breastfeeding, pregnant and potentially fertile women participant
Item
breastfeeding, pregnant and potentially fertile women participant.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C1960468 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C1960468 (UMLS CUI [3])
participants with insanity
Item
participants with insanity
boolean
C0004936 (UMLS CUI [1])
known allergies
Item
known allergies with shenfu zhusheye or its ingredients in the past.
boolean
C0020517 (UMLS CUI [1])
participants who have taken part in other clinical trials in last month
Item
participants who have taken part in other clinical trials in last month.
boolean
C2348568 (UMLS CUI [1])
participants who abuse alcohol or other drugs in last year
Item
participants who abuse alcohol or other drugs in last year.
boolean
C0038586 (UMLS CUI [1])
participants who are not suitable for clinical trial under doctors' consideration
Item
participants who are not suitable for clinical trial under doctors' consideration.
boolean
C0525058 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])