ID
16877
Description
Pexelizumab in Patients Undergoing Coronary Artery Bypass Grafting With Cardiopulmonary Bypass (PRIMO-CABG II); ODM derived from: https://clinicaltrials.gov/show/NCT00088179
Link
https://clinicaltrials.gov/show/NCT00088179
Keywords
Versions (2)
- 8/11/16 8/11/16 -
- 8/11/16 8/11/16 -
Uploaded on
August 11, 2016
DOI
To request one please log in.
License
Creative Commons BY 4.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Eligibility Coronary Artery Disease NCT00088179
Eligibility Coronary Artery Disease NCT00088179
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Salvage procedure Patient need for | Cardiopulmonary Resuscitation Continuous
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0442967
- UMLS CUI [1,2]
- C0686904
- UMLS CUI [2,1]
- C0007203
- UMLS CUI [2,2]
- C0549178
Description
Shock, Cardiogenic | Myocardial rupture left ventricle | Acute ventricular septal rupture | Rupture of papillary muscle
Data type
boolean
Alias
- UMLS CUI [1]
- C0036980
- UMLS CUI [2,1]
- C0018813
- UMLS CUI [2,2]
- C1269892
- UMLS CUI [3]
- C1299445
- UMLS CUI [4]
- C0155713
Description
Bacterial Infection Clinical Significance | Communicable Disease Clinical Significance | evaluation of evidence | White Blood Cell Count procedure | Body Temperature | Laboratory culture
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0004623
- UMLS CUI [1,2]
- C2826293
- UMLS CUI [2,1]
- C0009450
- UMLS CUI [2,2]
- C2826293
- UMLS CUI [3]
- C1327779
- UMLS CUI [4]
- C0023508
- UMLS CUI [5]
- C0005903
- UMLS CUI [6]
- C0430400
Description
hereditary serum complement deficiency
Data type
boolean
Alias
- UMLS CUI [1]
- C2030722
Description
Study Subject Participation Status | Investigational New Drugs Exposure to | Investigational Medical Device Exposure to
Data type
boolean
Alias
- UMLS CUI [1]
- C2348568
- UMLS CUI [2,1]
- C0013230
- UMLS CUI [2,2]
- C0332157
- UMLS CUI [3,1]
- C2346570
- UMLS CUI [3,2]
- C0332157
Description
Investigational New Drug Receive | Investigational Medical Device Receive | Study Subject Participation Status
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0013230
- UMLS CUI [1,2]
- C1514756
- UMLS CUI [2,1]
- C2346570
- UMLS CUI [2,2]
- C1514756
- UMLS CUI [3]
- C2348568
Description
Pregnancy | Breast Feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Similar models
Eligibility Coronary Artery Disease NCT00088179
- StudyEvent: Eligibility
C1265611 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C0205341 (UMLS CUI [2,2])
C1948041 (UMLS CUI [3,1])
C0439609 (UMLS CUI [3,2])
C0019993 (UMLS CUI [4,1])
C0678226 (UMLS CUI [4,2])
C3843040 (UMLS CUI [4,3])
C0027051 (UMLS CUI [5])
C1320718 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0007787 (UMLS CUI [4])
C0014099 (UMLS CUI [5])
C0018802 (UMLS CUI [6])
C1275491 (UMLS CUI [7])
C0027051 (UMLS CUI [8,1])
C1265611 (UMLS CUI [8,2])
C0010055 (UMLS CUI [9])
C0686904 (UMLS CUI [1,2])
C0007203 (UMLS CUI [2,1])
C0549178 (UMLS CUI [2,2])
C0018813 (UMLS CUI [2,1])
C1269892 (UMLS CUI [2,2])
C1299445 (UMLS CUI [3])
C0155713 (UMLS CUI [4])
C2826293 (UMLS CUI [1,2])
C0009450 (UMLS CUI [2,1])
C2826293 (UMLS CUI [2,2])
C1327779 (UMLS CUI [3])
C0023508 (UMLS CUI [4])
C0005903 (UMLS CUI [5])
C0430400 (UMLS CUI [6])
C0013230 (UMLS CUI [2,1])
C0332157 (UMLS CUI [2,2])
C2346570 (UMLS CUI [3,1])
C0332157 (UMLS CUI [3,2])
C1514756 (UMLS CUI [1,2])
C2346570 (UMLS CUI [2,1])
C1514756 (UMLS CUI [2,2])
C2348568 (UMLS CUI [3])
C0006147 (UMLS CUI [2])