ID
18318
Beschreibung
A Safety and Efficacy Trial Evaluating the Use of Fondaparinux in Percutaneous Coronary Intervention (PCI)(63133)(WITHDRAWN); ODM derived from: https://clinicaltrials.gov/show/NCT00060554
Link
https://clinicaltrials.gov/show/NCT00060554
Stichworte
Versionen (1)
- 30.10.16 30.10.16 -
Hochgeladen am
30. Oktober 2016
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Myocardial Infarction NCT00060554
Eligibility Myocardial Infarction NCT00060554
- StudyEvent: Eligibility
Beschreibung
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschreibung
Age
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0001779
Beschreibung
Activated clotting time measurement
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0427611
Beschreibung
Heparin, Low-Molecular-Weight
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0019139
Beschreibung
oral anticoagulants | International Normalized Ratio
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0354604
- UMLS CUI [2]
- C0525032
Beschreibung
Thrombolytic Therapy ST segment elevation myocardial infarction
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0040044
- UMLS CUI [1,2]
- C1536220
Beschreibung
Internal hemorrhage | Bleeding tendency
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1390214
- UMLS CUI [2]
- C1458140
Beschreibung
Thrombocytopenia | Platelet Count measurement
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0040034
- UMLS CUI [2]
- C0032181
Beschreibung
Pregnancy | Childbearing Potential Contraceptive methods Lacking
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2,1]
- C3831118
- UMLS CUI [2,2]
- C0700589
- UMLS CUI [2,3]
- C0332268
Beschreibung
Hypersensitivity Heparin | Hypersensitivity fondaparinux | Hypersensitivity Aspirin | Hypersensitivity clopidogrel
Datentyp
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
Beschreibung
Medical contraindication Absolute Anticoagulation Therapy
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0205344
- UMLS CUI [1,3]
- C0003281
Beschreibung
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Datentyp
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2]
- C0013230
- UMLS CUI [3]
- C2346570
Ähnliche Modelle
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])