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