Informations:
Erreur:
ID
29578
Description
A Phase I/II Clinical Study of SK&F-105517-D in Japanese Patients With Chronic Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00742508
Lien
https://clinicaltrials.gov/show/NCT00742508
Mots-clés
Versions (1)
- 07/04/2018 07/04/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
7 avril 2018
DOI
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Licence
Creative Commons BY 4.0
Modèle Commentaires :
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Eligibility Heart Failure, Congestive NCT00742508
Eligibility Heart Failure, Congestive NCT00742508
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure, Congestive NCT00742508
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Chronic heart failure Symptomatic Stable | Myocardial Ischemia | Cardiomyopathy, Dilated
Item
patients with symptomatically stable chronic heart failure (chf) based on ischemic heart disease or dilated cardiomyopathy
boolean
C0264716 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0151744 (UMLS CUI [2])
C0007193 (UMLS CUI [3])
C0231220 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0151744 (UMLS CUI [2])
C0007193 (UMLS CUI [3])
Maintenance therapy Heart failure | Angiotensin-Converting Enzyme Inhibitors Dosage unchanged | Angiotensin II receptor antagonist Dosage unchanged
Item
patients who are maintained on basic heart failure therapy with angiotensin converting enzyme (ace) inhibitors or angiotensin ii receptor blocker (arb) and their dosage/administration is not changed within 2 weeks
boolean
C0677908 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0003015 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0442739 (UMLS CUI [2,3])
C0521942 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0442739 (UMLS CUI [3,3])
C0018801 (UMLS CUI [1,2])
C0003015 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0442739 (UMLS CUI [2,3])
C0521942 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0442739 (UMLS CUI [3,3])
New York Heart Association Classification
Item
patients diagnosed with new york heart association (nyha) class i to iii
boolean
C1275491 (UMLS CUI [1])
Left ventricular ejection fraction
Item
patients with a left ventricular ejection fraction (lvef) between 25% and 45%
boolean
C0428772 (UMLS CUI [1])
Medical contraindication Adrenergic beta-1 Receptor Antagonists
Item
patients contraindicated for ß-blockers
boolean
C1301624 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
C0304516 (UMLS CUI [1,2])
Myocardial Infarction
Item
patients with occurrence of acute myocardial infarction within 2 weeks
boolean
C0027051 (UMLS CUI [1])
Angina, Unstable | Coronary spastic angina | Angina Pectoris At rest
Item
patients with unstable angina, coronary spastic angina, or angina at rest
boolean
C0002965 (UMLS CUI [1])
C0948698 (UMLS CUI [2])
C0002962 (UMLS CUI [3,1])
C0443144 (UMLS CUI [3,2])
C0948698 (UMLS CUI [2])
C0002962 (UMLS CUI [3,1])
C0443144 (UMLS CUI [3,2])
Collection of blood Amount Timespan
Item
patients who have collected blood >400 ml within 4 months prior to screening or >200 ml within 1 months
boolean
C0005834 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0872291 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,2])
C0872291 (UMLS CUI [1,3])