ID
42746
Description
A Study to Explore the Efficacy of TRV027 in Patients Hospitalized for Acute Decompensated Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT01966601
Lien
https://clinicaltrials.gov/show/NCT01966601
Mots-clés
Versions (2)
- 03/12/2015 03/12/2015 -
- 17/09/2021 17/09/2021 -
Téléchargé le
17 septembre 2021
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Acute Decompensated Heart Failure NCT01966601
Eligibility Acute Decompensated Heart Failure NCT01966601
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
pregnant or breast-feeding
Type de données
boolean
Alias
- UMLS CUI [1]
- C0549206
- UMLS CUI [2]
- C0006147
Description
acs in the 3 months prior to screening
Type de données
boolean
Alias
- UMLS CUI [1]
- C0948089
Description
Fever
Type de données
boolean
Alias
- UMLS CUI [1]
- C0015967
Description
clinically significant anemia
Type de données
boolean
Alias
- UMLS CUI [1]
- C0002871
Description
current or planned ultrafiltration, paracentesis, hemofiltration or dialysis
Type de données
boolean
Alias
- UMLS CUI [1]
- C0041612
- UMLS CUI [2]
- C0019014
- UMLS CUI [3]
- C0011946
- UMLS CUI [4]
- C0034115
Description
mechanical ventilation
Type de données
boolean
Alias
- UMLS CUI [1]
- C0199470
Description
cpap/bipap discontinued less than 1 hour prior to randomization
Type de données
boolean
Alias
- UMLS CUI [1]
- C0199451
- UMLS CUI [2]
- C1956423
Description
primary pulmonary hypertension
Type de données
boolean
Alias
- UMLS CUI [1]
- C0152171
Description
history or current use of left ventricular assist devices (lvads) or intra-aortic balloon pumps (iabps)
Type de données
boolean
Alias
- UMLS CUI [1]
- C0181598
- UMLS CUI [2]
- C0702122
Description
intravenous radiographic contrast agent within 72 hours prior to screening or presence of acute contrast induced nephropathy at the time of screening
Type de données
boolean
Alias
- UMLS CUI [1]
- C0742799
- UMLS CUI [2]
- C0268775
Description
arrhythmia
Type de données
boolean
Alias
- UMLS CUI [1]
- C0003811
Description
nitroprusside or nesiritide
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
intravenous nitrates
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
use of inotropes
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
use of arbs within 7 days of prior to randomization
Type de données
boolean
Alias
- UMLS CUI [1]
- C2347852
Description
use of any investigational medication within 30 days
Type de données
boolean
Alias
- UMLS CUI [1]
- C2348568
Description
clinically significant hypersensitivity or allergy to, or intolerance of, angiotensin receptor blockers
Type de données
boolean
Alias
- UMLS CUI [1]
- C0020517
- UMLS CUI [2]
- C0521942
Description
major surgery
Type de données
boolean
Alias
- UMLS CUI [1]
- C0679637
Description
stroke
Type de données
boolean
Alias
- UMLS CUI [1]
- C0038454
Description
egfr (smdrd) <20 ml/min/1.73m2 or >75 ml/min/1.73m2 between presentation and randomization
Type de données
boolean
Alias
- UMLS CUI [1]
- C3811844
Description
post cardiac or renal transplant
Type de données
boolean
Alias
- UMLS CUI [1]
- C0040732
Description
listed for transplant
Type de données
boolean
Alias
- UMLS CUI [1]
- C0040732
Description
history of severe left ventricular outlet obstruction (either valvular or sub-valvular), severe mitral valve stenosis or severe aortic regurgitation
Type de données
boolean
Alias
- UMLS CUI [1]
- C2919935
- UMLS CUI [2]
- C0026269
- UMLS CUI [3]
- C0003504
Description
cardiac valvular abnormality
Type de données
boolean
Alias
- UMLS CUI [1]
- C1859330
Description
congenital heart disease
Type de données
boolean
Alias
- UMLS CUI [1]
- C0152021
Description
hypertrophic or restrictive cardiomyopathy
Type de données
boolean
Alias
- UMLS CUI [1]
- C0878544
Description
significant pulmonary or hepatic disease that could interfere with the evaluation of safety or efficacy of trv027
Type de données
boolean
Alias
- UMLS CUI [1]
- C0525058
- UMLS CUI [2]
- C0439801
- UMLS CUI [3]
- C0009488
Description
life expectancy
Type de données
boolean
Alias
- UMLS CUI [1]
- C0023671
Similar models
Eligibility Acute Decompensated Heart Failure NCT01966601
- StudyEvent: Eligibility
C0011900 (UMLS CUI [2])
C0741286 (UMLS CUI [2])
C3272900 (UMLS CUI [2])
C1095989 (UMLS CUI [2])
C3272900 (UMLS CUI [3])
C1095989 (UMLS CUI [2])
C3272900 (UMLS CUI [3])
C1391960 (UMLS CUI [2])
C0231807 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C0019014 (UMLS CUI [2])
C0011946 (UMLS CUI [3])
C0034115 (UMLS CUI [4])
C1956423 (UMLS CUI [2])
C0702122 (UMLS CUI [2])
C0268775 (UMLS CUI [2])
C0521942 (UMLS CUI [2])
C0026269 (UMLS CUI [2])
C0003504 (UMLS CUI [3])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
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