ID
11733
Beschrijving
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.
Trefwoorden
Versies (2)
- 28-07-15 28-07-15 -
- 21-11-15 21-11-15 -
Geüploaded op
28 juli 2015
DOI
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Licentie
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
Beschrijving
Exclusion criteria
Beschrijving
ST elevated myocardial infarction within the preceding 48 hours
Datatype
boolean
Alias
- UMLS CUI-1
- C1536220
Beschrijving
Patient weighs more than 400 lbs (181.2 kg) or less than 110 lbs (50 kg)
Datatype
boolean
Alias
- UMLS CUI-1
- C0005910
Beschrijving
Patients presenting on or received bivalirudin within the preceding 24 hours;
Datatype
boolean
Alias
- UMLS CUI-1
- C0168273
Beschrijving
Patients presenting on or received GP IIb/IIIa inhibitors within the preceding 24 hours;
Datatype
boolean
Alias
- UMLS CUI-1
- C3640054
Beschrijving
Patients presenting on or received low-molecular weight heparin within the preceding 24 hours
Datatype
boolean
Alias
- UMLS CUI-1
- C3536766
Beschrijving
Patients that received unfractionated heparin less than or equal to 90 minutes prior to fondaparinux administration.
Datatype
boolean
Alias
- UMLS CUI-1
- C2825026
Beschrijving
Patients with known conditions of bleeding diathesis
Datatype
boolean
Alias
- UMLS CUI-1
- C3251812
Beschrijving
Patients with actively bleeding within the previous 6 months (GI bleed etc.);
Datatype
boolean
Alias
- UMLS CUI-1
- C0019080
Beschrijving
Known diagnosis of acute bacterial endocarditis;
Datatype
boolean
Alias
- UMLS CUI-1
- C0014121
Beschrijving
Patients with cardiogenic shock
Datatype
boolean
Alias
- UMLS CUI-1
- C0036980
Beschrijving
Required intra-aortic balloon pump (IABP)
Datatype
boolean
Alias
- UMLS CUI-1
- C0021860
Beschrijving
If patient is on warfarin (Coumadin) therapy
Datatype
boolean
Alias
- UMLS CUI-1
- C0043031
Beschrijving
Patients who had a major or minor stroke (CVA or TIA)
Datatype
boolean
Alias
- UMLS CUI-1
- C0559159
Beschrijving
Patients who had a major surgery within the past 6 months;
Datatype
boolean
Alias
- UMLS CUI-1
- C0679637
Beschrijving
Known impaired renal function (creatinine ≥ 3.0 mg/dL (265.2 μmol/L)
Datatype
boolean
Alias
- UMLS CUI-1
- C0035078
Beschrijving
status post renal transplant
Datatype
boolean
Alias
- UMLS CUI-1
- C0022671
Beschrijving
patients on chronic dialysis
Datatype
boolean
Alias
- UMLS CUI-1
- C0019004
Beschrijving
creatinine clearance ≤ 30 ml/min
Datatype
boolean
Alias
- UMLS CUI-1
- C0373595
Beschrijving
A platelet count of less than 100,000 cells/mm3;
Datatype
boolean
Alias
- UMLS CUI-1
- C0032181
Beschrijving
Known allergies to fondaparinux, aspirin, clopidogrel bisulfate (PlavixR), ticlopidine (TiclidR), heparin, bivalirudin, that cannot be medically managed;
Datatype
boolean
Alias
- UMLS CUI-1
- C0013182
Beschrijving
Known allergies to contrast that cannot be medically managed;
Datatype
boolean
Alias
- UMLS CUI-1
- C0570562
Beschrijving
Prior angioplasty within the previous 30 days;
Datatype
boolean
Alias
- UMLS CUI-1
- C3532648
Beschrijving
Contraindication to low-molecular weight heparin
Datatype
boolean
Alias
- UMLS CUI-1
- C3536766
- UMLS CUI-2
- C0522473
- UMLS CUI-3
- P
Beschrijving
Contraindication to unfractionated heparin
Datatype
boolean
Alias
- UMLS CUI-1
- C2825026
- UMLS CUI-2
- C0522473
- UMLS CUI-3
- P
Beschrijving
Contraindication to bivalirudin;
Datatype
boolean
Alias
- UMLS CUI-1
- C0168273
- UMLS CUI-2
- C0522473
- UMLS CUI-3
- P
Beschrijving
Pregnant or lactating women;
Datatype
boolean
Alias
- UMLS CUI-1
- C0549206
Beschrijving
Pregnant or lactating women;
Datatype
boolean
Alias
- UMLS CUI-1
- C2828358
Beschrijving
Currently participating in an investigational drug or another device study.
Datatype
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)