ID

42658

Descrizione

Radial Artery Versus Saphenous Vein Grafts in Coronary Artery Bypass Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT00054847

collegamento

https://clinicaltrials.gov/show/NCT00054847

Keywords

versioni (2)
  1. 23/07/16 23/07/16 -
  2. 17/09/21 17/09/21 -
Caricato su

17 settembre 2021

DOI

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Licenza

Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT00054847

Inglese

Eligibility Cardiovascular Disease NCT00054847

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients needing coronary artery bypass grafts.
Descrizione

Coronary Artery Bypass Surgery Patient need for

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C0686904
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who require only a single vessel bypass and in whom the internal mammary artery will be used for that graft
Descrizione

Single vessel bypass graft Requirement | Graft Using internal mammary artery

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0853481
UMLS CUI [1,2]
C1514873
UMLS CUI [2,1]
C0332835
UMLS CUI [2,2]
C1524063
UMLS CUI [2,3]
C1269885
patients with previous stripping and ligation of saphenous veins and in whom no venous conduit is available for bypass
Descrizione

Saphenous Vein Stripping and ligation | Vein Available Bypass

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0036186
UMLS CUI [1,2]
C0185048
UMLS CUI [2,1]
C0042449
UMLS CUI [2,2]
C0470187
UMLS CUI [2,3]
C0741847
patients with raynaud's symptoms
Descrizione

Raynaud Disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0034734
patients who have a creatinine above 2.0 mg/dl or require hemodialysis
Descrizione

Creatinine measurement, serum | Hemodialysis Requirement

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2,1]
C0019004
UMLS CUI [2,2]
C1514873
patients with a positive allen test
Descrizione

Allen test Positive

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0231664
UMLS CUI [1,2]
C1446409
patients with cardiogenic shock
Descrizione

Shock, Cardiogenic

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0036980
patients who are unable to give consent
Descrizione

Informed Consent Unable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
patients allergic to contrast material
Descrizione

Hypersensitivity Contrast Media

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0009924
patients undergoing repeat cabg or any form of robotic surgery
Descrizione

Coronary Artery Bypass Surgery Repeat | Robotic assisted surgery

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0010055
UMLS CUI [1,2]
C0205341
UMLS CUI [2]
C3850136
patients who do not have full use of both arms
Descrizione

Ability to move Upper Extremities

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0344382
UMLS CUI [1,2]
C1140618
patients who are pregnant
Descrizione

Pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
patients with neurologic or musculoskeletal disease affecting the arm
Descrizione

nervous system disorder Affecting Upper Extremity | Musculoskeletal Disease Affecting Upper Extremity

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0027765
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C1140618
UMLS CUI [2,1]
C0026857
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C1140618
patients who refuse to participate
Descrizione

Refusal to Participate

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1136454
patient requires any concomitant valve operation in the mitral, aortic, or pulmonary position. isolated tricuspid annuloplasty is acceptable, but tricuspid valve replacement excludes the patient from consideration.
Descrizione

Mitral Valve Requirement Operative Surgical Procedures | Aortic valve Requirement Operative Surgical Procedures | Pulmonary valve Requirement Operative Surgical Procedures | Annuloplasty of tricuspid valve Isolated | Replacement of tricuspid valve

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0026264
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0543467
UMLS CUI [2,1]
C0003501
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0543467
UMLS CUI [3,1]
C0034086
UMLS CUI [3,2]
C1514873
UMLS CUI [3,3]
C0543467
UMLS CUI [4,1]
C0396902
UMLS CUI [4,2]
C0205409
UMLS CUI [5]
C0190119
patient requires concomitant dor or maze procedure
Descrizione

Surgical ventricular restoration procedure (SVR, Dor procedures) Requirement | Maze procedure Requirement

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1611753
UMLS CUI [1,2]
C1514873
UMLS CUI [2,1]
C0397414
UMLS CUI [2,2]
C1514873
patient is in another research study
Descrizione

Study Subject Participation Status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2348568
no suitable radial target (there is no non-lad vessel with a >70% stenosis)
Descrizione

radial artery Target suitable | Left anterior descending coronary artery stenosis

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0162857
UMLS CUI [1,2]
C1521840
UMLS CUI [1,3]
C3900053
UMLS CUI [2]
C3267165
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Similar models

Eligibility Cardiovascular Disease NCT00054847

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Coronary Artery Bypass Surgery Patient need for
Item
patients needing coronary artery bypass grafts.
boolean
C0010055 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Single vessel bypass graft Requirement | Graft Using internal mammary artery
Item
patients who require only a single vessel bypass and in whom the internal mammary artery will be used for that graft
boolean
C0853481 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0332835 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
C1269885 (UMLS CUI [2,3])
Saphenous Vein Stripping and ligation | Vein Available Bypass
Item
patients with previous stripping and ligation of saphenous veins and in whom no venous conduit is available for bypass
boolean
C0036186 (UMLS CUI [1,1])
C0185048 (UMLS CUI [1,2])
C0042449 (UMLS CUI [2,1])
C0470187 (UMLS CUI [2,2])
C0741847 (UMLS CUI [2,3])
Raynaud Disease
Item
patients with raynaud's symptoms
boolean
C0034734 (UMLS CUI [1])
Creatinine measurement, serum | Hemodialysis Requirement
Item
patients who have a creatinine above 2.0 mg/dl or require hemodialysis
boolean
C0201976 (UMLS CUI [1])
C0019004 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
Allen test Positive
Item
patients with a positive allen test
boolean
C0231664 (UMLS CUI [1,1])
C1446409 (UMLS CUI [1,2])
Shock, Cardiogenic
Item
patients with cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
Informed Consent Unable
Item
patients who are unable to give consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Hypersensitivity Contrast Media
Item
patients allergic to contrast material
boolean
C0020517 (UMLS CUI [1,1])
C0009924 (UMLS CUI [1,2])
Coronary Artery Bypass Surgery Repeat | Robotic assisted surgery
Item
patients undergoing repeat cabg or any form of robotic surgery
boolean
C0010055 (UMLS CUI [1,1])
C0205341 (UMLS CUI [1,2])
C3850136 (UMLS CUI [2])
Ability to move Upper Extremities
Item
patients who do not have full use of both arms
boolean
C0344382 (UMLS CUI [1,1])
C1140618 (UMLS CUI [1,2])
Pregnancy
Item
patients who are pregnant
boolean
C0032961 (UMLS CUI [1])
nervous system disorder Affecting Upper Extremity | Musculoskeletal Disease Affecting Upper Extremity
Item
patients with neurologic or musculoskeletal disease affecting the arm
boolean
C0027765 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C1140618 (UMLS CUI [1,3])
C0026857 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C1140618 (UMLS CUI [2,3])
Refusal to Participate
Item
patients who refuse to participate
boolean
C1136454 (UMLS CUI [1])
Mitral Valve Requirement Operative Surgical Procedures | Aortic valve Requirement Operative Surgical Procedures | Pulmonary valve Requirement Operative Surgical Procedures | Annuloplasty of tricuspid valve Isolated | Replacement of tricuspid valve
Item
patient requires any concomitant valve operation in the mitral, aortic, or pulmonary position. isolated tricuspid annuloplasty is acceptable, but tricuspid valve replacement excludes the patient from consideration.
boolean
C0026264 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,3])
C0003501 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0543467 (UMLS CUI [2,3])
C0034086 (UMLS CUI [3,1])
C1514873 (UMLS CUI [3,2])
C0543467 (UMLS CUI [3,3])
C0396902 (UMLS CUI [4,1])
C0205409 (UMLS CUI [4,2])
C0190119 (UMLS CUI [5])
Surgical ventricular restoration procedure (SVR, Dor procedures) Requirement | Maze procedure Requirement
Item
patient requires concomitant dor or maze procedure
boolean
C1611753 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0397414 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
Study Subject Participation Status
Item
patient is in another research study
boolean
C2348568 (UMLS CUI [1])
radial artery Target suitable | Left anterior descending coronary artery stenosis
Item
no suitable radial target (there is no non-lad vessel with a >70% stenosis)
boolean
C0162857 (UMLS CUI [1,1])
C1521840 (UMLS CUI [1,2])
C3900053 (UMLS CUI [1,3])
C3267165 (UMLS CUI [2])
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