ID
11733
Beskrivning
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.
Nyckelord
Versioner (2)
- 2015-07-28 2015-07-28 -
- 2015-11-21 2015-11-21 -
Uppladdad den
28 juli 2015
DOI
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Licens
Creative Commons BY-NC 3.0 Legacy
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Eligibility Criteria: Switching From Fondaparinux to Bivalirudin or Unfractionated Heparin in ACS Patients Undergoing PCI (SWITCHIII)
Eligibility Criteria
- StudyEvent: ODM
Beskrivning
Exclusion criteria
Beskrivning
ST elevated myocardial infarction within the preceding 48 hours
Datatyp
boolean
Alias
- UMLS CUI-1
- C1536220
Beskrivning
Patient weighs more than 400 lbs (181.2 kg) or less than 110 lbs (50 kg)
Datatyp
boolean
Alias
- UMLS CUI-1
- C0005910
Beskrivning
Patients presenting on or received bivalirudin within the preceding 24 hours;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0168273
Beskrivning
Patients presenting on or received GP IIb/IIIa inhibitors within the preceding 24 hours;
Datatyp
boolean
Alias
- UMLS CUI-1
- C3640054
Beskrivning
Patients presenting on or received low-molecular weight heparin within the preceding 24 hours
Datatyp
boolean
Alias
- UMLS CUI-1
- C3536766
Beskrivning
Patients that received unfractionated heparin less than or equal to 90 minutes prior to fondaparinux administration.
Datatyp
boolean
Alias
- UMLS CUI-1
- C2825026
Beskrivning
Patients with known conditions of bleeding diathesis
Datatyp
boolean
Alias
- UMLS CUI-1
- C3251812
Beskrivning
Patients with actively bleeding within the previous 6 months (GI bleed etc.);
Datatyp
boolean
Alias
- UMLS CUI-1
- C0019080
Beskrivning
Known diagnosis of acute bacterial endocarditis;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0014121
Beskrivning
Patients with cardiogenic shock
Datatyp
boolean
Alias
- UMLS CUI-1
- C0036980
Beskrivning
Required intra-aortic balloon pump (IABP)
Datatyp
boolean
Alias
- UMLS CUI-1
- C0021860
Beskrivning
If patient is on warfarin (Coumadin) therapy
Datatyp
boolean
Alias
- UMLS CUI-1
- C0043031
Beskrivning
Patients who had a major or minor stroke (CVA or TIA)
Datatyp
boolean
Alias
- UMLS CUI-1
- C0559159
Beskrivning
Patients who had a major surgery within the past 6 months;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0679637
Beskrivning
Known impaired renal function (creatinine ≥ 3.0 mg/dL (265.2 μmol/L)
Datatyp
boolean
Alias
- UMLS CUI-1
- C0035078
Beskrivning
status post renal transplant
Datatyp
boolean
Alias
- UMLS CUI-1
- C0022671
Beskrivning
patients on chronic dialysis
Datatyp
boolean
Alias
- UMLS CUI-1
- C0019004
Beskrivning
creatinine clearance ≤ 30 ml/min
Datatyp
boolean
Alias
- UMLS CUI-1
- C0373595
Beskrivning
A platelet count of less than 100,000 cells/mm3;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0032181
Beskrivning
Known allergies to fondaparinux, aspirin, clopidogrel bisulfate (PlavixR), ticlopidine (TiclidR), heparin, bivalirudin, that cannot be medically managed;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0013182
Beskrivning
Known allergies to contrast that cannot be medically managed;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0570562
Beskrivning
Prior angioplasty within the previous 30 days;
Datatyp
boolean
Alias
- UMLS CUI-1
- C3532648
Beskrivning
Contraindication to low-molecular weight heparin
Datatyp
boolean
Alias
- UMLS CUI-1
- C3536766
- UMLS CUI-2
- C0522473
- UMLS CUI-3
- P
Beskrivning
Contraindication to unfractionated heparin
Datatyp
boolean
Alias
- UMLS CUI-1
- C2825026
- UMLS CUI-2
- C0522473
- UMLS CUI-3
- P
Beskrivning
Contraindication to bivalirudin;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0168273
- UMLS CUI-2
- C0522473
- UMLS CUI-3
- P
Beskrivning
Pregnant or lactating women;
Datatyp
boolean
Alias
- UMLS CUI-1
- C0549206
Beskrivning
Pregnant or lactating women;
Datatyp
boolean
Alias
- UMLS CUI-1
- C2828358
Beskrivning
Currently participating in an investigational drug or another device study.
Datatyp
boolean
Alias
- UMLS CUI-1
- C0422740
Similar models
Eligibility Criteria
- StudyEvent: ODM
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)
C0522473 (UMLS CUI-2)
P (UMLS CUI-3)