ID
12472
Description
The primary objective of this clinical trial is to evaluate safety of switching from fondaparinux to either unfractionated heparin or bivalirudin for patients experiencing acute coronary syndrome undergoing percutaneous coronary angioplasty. https://clinicaltrials.gov/ct2/show/NCT00464087
Link
https://clinicaltrials.gov/ct2/show/NCT00464087
Keywords
Versions (2)
- 7/28/15 7/28/15 -
- 11/21/15 11/21/15 -
Uploaded on
November 21, 2015
DOI
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License
Creative Commons BY 4.0
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Eligibility SWITCHIII Acute Coronary Syndrome NCT00464087
Eligibility Criteria
- StudyEvent: ODM
Description
Exclusion criteria
Description
ST elevated myocardial infarction within the preceding 48 hours
Data type
boolean
Alias
- UMLS CUI-1
- C1536220
Description
Patient weighs more than 400 lbs (181.2 kg) or less than 110 lbs (50 kg)
Data type
boolean
Alias
- UMLS CUI-1
- C0005910
Description
Patients presenting on or received bivalirudin within the preceding 24 hours;
Data type
boolean
Alias
- UMLS CUI-1
- C0168273
Description
Patients presenting on or received GP IIb/IIIa inhibitors within the preceding 24 hours;
Data type
boolean
Alias
- UMLS CUI-1
- C3640054
Description
Patients presenting on or received low-molecular weight heparin within the preceding 24 hours
Data type
boolean
Alias
- UMLS CUI-1
- C3536766
Description
Patients that received unfractionated heparin less than or equal to 90 minutes prior to fondaparinux administration.
Data type
boolean
Alias
- UMLS CUI-1
- C2825026
Description
Patients with known conditions of bleeding diathesis
Data type
boolean
Alias
- UMLS CUI-1
- C3251812
Description
Patients with actively bleeding within the previous 6 months (GI bleed etc.);
Data type
boolean
Alias
- UMLS CUI-1
- C0019080
Description
Known diagnosis of acute bacterial endocarditis;
Data type
boolean
Alias
- UMLS CUI-1
- C0014121
Description
Patients with cardiogenic shock
Data type
boolean
Alias
- UMLS CUI-1
- C0036980
Description
Required intra-aortic balloon pump (IABP)
Data type
boolean
Alias
- UMLS CUI-1
- C0021860
Description
If patient is on warfarin (Coumadin) therapy
Data type
boolean
Alias
- UMLS CUI-1
- C0043031
Description
Patients who had a major or minor stroke (CVA or TIA)
Data type
boolean
Alias
- UMLS CUI-1
- C0559159
Description
Patients who had a major surgery within the past 6 months;
Data type
boolean
Alias
- UMLS CUI-1
- C0679637
Description
Known impaired renal function (creatinine ≥ 3.0 mg/dL (265.2 μmol/L)
Data type
boolean
Alias
- UMLS CUI-1
- C0035078
Description
status post renal transplant
Data type
boolean
Alias
- UMLS CUI-1
- C0022671
Description
patients on chronic dialysis
Data type
boolean
Alias
- UMLS CUI-1
- C0019004
Description
creatinine clearance ≤ 30 ml/min
Data type
boolean
Alias
- UMLS CUI-1
- C0373595
Description
A platelet count of less than 100,000 cells/mm3;
Data type
boolean
Alias
- UMLS CUI-1
- C0032181
Description
Known allergies to fondaparinux, aspirin, clopidogrel bisulfate (PlavixR), ticlopidine (TiclidR), heparin, bivalirudin, that cannot be medically managed;
Data type
boolean
Alias
- UMLS CUI-1
- C0013182
Description
Known allergies to contrast that cannot be medically managed;
Data type
boolean
Alias
- UMLS CUI-1
- C0570562
Description
Prior angioplasty within the previous 30 days;
Data type
boolean
Alias
- UMLS CUI-1
- C3532648
Description
Contraindication to low-molecular weight heparin
Data type
boolean
Alias
- UMLS CUI [1,1]
- C3536766
- UMLS CUI [1,2]
- C0522473
Description
Contraindication to unfractionated heparin
Data type
boolean
Alias
- UMLS CUI [1,1]
- C2825026
- UMLS CUI [1,2]
- C0522473
Description
Contraindication to bivalirudin;
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0168273
- UMLS CUI [1,2]
- C0522473
Description
Pregnant or lactating women;
Data type
boolean
Alias
- UMLS CUI-1
- C0549206
Description
Pregnant or lactating women;
Data type
boolean
Alias
- UMLS CUI-1
- C2828358
Description
Currently participating in an investigational drug or another device study.
Data type
boolean
Alias
- UMLS CUI-1
- C0422740
Similar models
Eligibility Criteria
- StudyEvent: ODM
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])
C0522473 (UMLS CUI [1,2])