ID
18318
Description
A Safety and Efficacy Trial Evaluating the Use of Fondaparinux in Percutaneous Coronary Intervention (PCI)(63133)(WITHDRAWN); ODM derived from: https://clinicaltrials.gov/show/NCT00060554
Lien
https://clinicaltrials.gov/show/NCT00060554
Mots-clés
Versions (1)
- 30/10/2016 30/10/2016 -
Téléchargé le
30 octobre 2016
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Myocardial Infarction NCT00060554
Eligibility Myocardial Infarction NCT00060554
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Age
Type de données
boolean
Alias
- UMLS CUI [1]
- C0001779
Description
Activated clotting time measurement
Type de données
boolean
Alias
- UMLS CUI [1]
- C0427611
Description
Heparin, Low-Molecular-Weight
Type de données
boolean
Alias
- UMLS CUI [1]
- C0019139
Description
oral anticoagulants | International Normalized Ratio
Type de données
boolean
Alias
- UMLS CUI [1]
- C0354604
- UMLS CUI [2]
- C0525032
Description
Thrombolytic Therapy ST segment elevation myocardial infarction
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0040044
- UMLS CUI [1,2]
- C1536220
Description
Internal hemorrhage | Bleeding tendency
Type de données
boolean
Alias
- UMLS CUI [1]
- C1390214
- UMLS CUI [2]
- C1458140
Description
Thrombocytopenia | Platelet Count measurement
Type de données
boolean
Alias
- UMLS CUI [1]
- C0040034
- UMLS CUI [2]
- C0032181
Description
Pregnancy | Childbearing Potential Contraceptive methods Lacking
Type de données
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2,1]
- C3831118
- UMLS CUI [2,2]
- C0700589
- UMLS CUI [2,3]
- C0332268
Description
Hypersensitivity Heparin | Hypersensitivity fondaparinux | Hypersensitivity Aspirin | Hypersensitivity clopidogrel
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0019134
- UMLS CUI [2,1]
- C0020517
- UMLS CUI [2,2]
- C1098510
- UMLS CUI [3,1]
- C0020517
- UMLS CUI [3,2]
- C0004057
- UMLS CUI [4,1]
- C0020517
- UMLS CUI [4,2]
- C0070166
Description
Medical contraindication Absolute Anticoagulation Therapy
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0205344
- UMLS CUI [1,3]
- C0003281
Description
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Type de données
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0013230
- UMLS CUI [3]
- C2346570
Similar models
Eligibility Myocardial Infarction NCT00060554
- StudyEvent: Eligibility
C1301732 (UMLS CUI [1,2])
C3160886 (UMLS CUI [2])
C1532338 (UMLS CUI [3,1])
C0205225 (UMLS CUI [3,2])
C1536220 (UMLS CUI [3,3])
C1532338 (UMLS CUI [4,1])
C0439608 (UMLS CUI [4,2])
C0018795 (UMLS CUI [5])
C0525032 (UMLS CUI [2])
C1536220 (UMLS CUI [1,2])
C1458140 (UMLS CUI [2])
C0032181 (UMLS CUI [2])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
C0019134 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1098510 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0004057 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0070166 (UMLS CUI [4,2])
C0205344 (UMLS CUI [1,2])
C0003281 (UMLS CUI [1,3])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])