ID
40861
Description
Phase 4 Study to Demonstrate Prognostic Usefulness of AdreView™ Scintigraphy for Identifying Subjects With Heart Failure Who Will Experience Death During 60 Months Follow-up.; ODM derived from: https://clinicaltrials.gov/show/NCT02127307
Lien
https://clinicaltrials.gov/show/NCT02127307
Mots-clés
Versions (1)
- 27/05/2020 27/05/2020 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
27 mai 2020
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Heart Failure (HF) NCT02127307
Eligibility Heart Failure (HF) NCT02127307
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Patient withdrawn from trial Specified
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0205369
Description
Heart Transplantation
Type de données
boolean
Alias
- UMLS CUI [1]
- C0018823
Description
Patient died
Type de données
boolean
Alias
- UMLS CUI [1]
- C1306577
Description
Patient withdrawn from trial Specified Voluntary
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0205369
- UMLS CUI [1,3]
- C0439656
Description
Study Subject Unavailable | Survival Status Information Lacking
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0681850
- UMLS CUI [1,2]
- C0686905
- UMLS CUI [2,1]
- C1148433
- UMLS CUI [2,2]
- C1533716
- UMLS CUI [2,3]
- C0332268
Similar models
Eligibility Heart Failure (HF) NCT02127307
- StudyEvent: Eligibility
C0205197 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,2])
C1550543 (UMLS CUI [1,3])
C0444454 (UMLS CUI [2,1])
C0025102 (UMLS CUI [2,2])
C1705116 (UMLS CUI [1,2])
C3827528 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
C0686905 (UMLS CUI [1,2])
C0444454 (UMLS CUI [2,1])
C0025102 (UMLS CUI [2,2])
C0205369 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,2])
C0439656 (UMLS CUI [1,3])
C0686905 (UMLS CUI [1,2])
C1148433 (UMLS CUI [2,1])
C1533716 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])