0 Ratings
ID

15920

Description

POISE Trial: Perioperative Ischemic Evaluation Study; ODM derived from: https://clinicaltrials.gov/show/NCT00182039

Link

https://clinicaltrials.gov/show/NCT00182039

Keywords

Versions (2)
  1. 6/5/16 6/5/16 -
  2. 6/18/16 6/18/16 -
Uploaded on

June 18, 2016

DOI

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License

Creative Commons BY 4.0
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    Eligibility Cardiovascular Diseases NCT00182039

    English

    Eligibility Cardiovascular Diseases NCT00182039

    1 forms  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    patients undergoing noncardiac surgery
    Description

    noncardiac surgery

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0543467
    UMLS CUI [1,2]
    C1522601
    UMLS CUI [1,3]
    C1518422
    ≥ 45 years of age; either sex.
    Description

    age

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    have an expected length of stay ≥ 24 hours
    Description

    in-patient duration

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0023303
    fulfill any one of the following 6 criteria:
    Description

    ID.4

    Data type

    boolean

    coronary artery disease;
    Description

    coronary artery disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C1956346
    peripheral vascular disease;
    Description

    peripheral vascular disease

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0085096
    history of stroke due to atherothrombotic disease;
    Description

    history of stroke

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C4039739
    hospitalization for congestive heart failure within 3 years of randomization;
    Description

    congestive heart failure

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0019993
    UMLS CUI [1,2]
    C0018802
    undergoing major vascular surgery; or
    Description

    major vascular surgery

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0042381
    any 3 of the following 7 criteria: scheduled for high risk surgery (i.e. intraperitoneal or intrathoracic); emergency/urgent surgery; any history of congestive heart failure; history of a transient ischemic attack (tia); diabetes and currently on an oral hypoglycemic agent or insulin therapy; preoperative serum creatinine > 175 µmol/l (> 2.0 mg/dl); or age > 70 years.
    Description

    informed consent; comorbidities

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C2216322
    UMLS CUI [2,1]
    C0018802
    UMLS CUI [2,2]
    C0262926
    UMLS CUI [3,1]
    C0007787
    UMLS CUI [3,2]
    C0262926
    UMLS CUI [4,1]
    C0011849
    UMLS CUI [4,2]
    C0020616
    UMLS CUI [4,3]
    C0557978
    UMLS CUI [5,1]
    C0201976
    UMLS CUI [5,2]
    C0445204
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    contraindication to metoprolol including any of the following: significant bradycardia (heart rate < 50 beats per minute); second or third degree heart block without a pacemaker; asthma that has been active within the last decade; and history of chronic obstructive pulmonary disease (copd) with bronchospasm on pulmonary function tests.
    Description

    contraindication to metoprolol

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0428977
    UMLS CUI [2]
    C0264906
    UMLS CUI [3]
    C0151517
    UMLS CUI [4]
    C0004096
    UMLS CUI [5]
    C0024117
    clinical plan to use a beta-blocker preoperatively or during the first 30 postoperative days
    Description

    beta-blocker usage

    Data type

    boolean

    Alias
    UMLS CUI [1]
    C0001645
    prior adverse reaction to a beta-blocker
    Description

    hypersensitivity to beta-blocker

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0020517
    UMLS CUI [1,2]
    C0001645
    coronary artery bypass graft (cabg) surgery with complete revascularization in the preceding 5 years and no evidence of cardiac ischemia since the cabg surgery
    Description

    cabg

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0010055
    UMLS CUI [1,2]
    C0151744
    UMLS CUI [1,3]
    C0332197
    patients undergoing low risk surgical procedures (potential examples include transurethral procedures [transurethral prostatectomies (turps), stone baskets, etc.], ophthalmologic procedures under topical or regional anesthesia [cornea transplants, cataract surgery, etc.], and surgeries with limited physiological stresses [digital re-implantation, nerve repairs, etc.] )
    Description

    low risk surgery

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0543467
    UMLS CUI [1,2]
    C3538919
    concurrent use of verapamil
    Description

    concurrent use of verapamil

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C0009429
    UMLS CUI [1,2]
    C0042523
    prior enrollment in this trial
    Description

    prior enrollment in this trial

    Data type

    boolean

    Alias
    UMLS CUI [1,1]
    C1516879
    UMLS CUI [1,2]
    C0332152
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    Similar models

    Eligibility Cardiovascular Diseases NCT00182039

    1 forms
    Name
    Type
    Description | Question | Decode (Coded Value)
    Data type
    Alias
    Item Group
    C1512693 (UMLS CUI)
    noncardiac surgery
    Item
    patients undergoing noncardiac surgery
    boolean
    C0543467 (UMLS CUI [1,1])
    C1522601 (UMLS CUI [1,2])
    C1518422 (UMLS CUI [1,3])
    age
    Item
    ≥ 45 years of age; either sex.
    boolean
    C0001779 (UMLS CUI [1])
    in-patient duration
    Item
    have an expected length of stay ≥ 24 hours
    boolean
    C0023303 (UMLS CUI [1])
    ID.4
    Item
    fulfill any one of the following 6 criteria:
    boolean
    coronary artery disease
    Item
    coronary artery disease;
    boolean
    C1956346 (UMLS CUI [1])
    peripheral vascular disease
    Item
    peripheral vascular disease;
    boolean
    C0085096 (UMLS CUI [1])
    history of stroke
    Item
    history of stroke due to atherothrombotic disease;
    boolean
    C4039739 (UMLS CUI [1])
    congestive heart failure
    Item
    hospitalization for congestive heart failure within 3 years of randomization;
    boolean
    C0019993 (UMLS CUI [1,1])
    C0018802 (UMLS CUI [1,2])
    major vascular surgery
    Item
    undergoing major vascular surgery; or
    boolean
    C0042381 (UMLS CUI [1])
    informed consent; comorbidities
    Item
    any 3 of the following 7 criteria: scheduled for high risk surgery (i.e. intraperitoneal or intrathoracic); emergency/urgent surgery; any history of congestive heart failure; history of a transient ischemic attack (tia); diabetes and currently on an oral hypoglycemic agent or insulin therapy; preoperative serum creatinine > 175 µmol/l (> 2.0 mg/dl); or age > 70 years.
    boolean
    C2216322 (UMLS CUI [1])
    C0018802 (UMLS CUI [2,1])
    C0262926 (UMLS CUI [2,2])
    C0007787 (UMLS CUI [3,1])
    C0262926 (UMLS CUI [3,2])
    C0011849 (UMLS CUI [4,1])
    C0020616 (UMLS CUI [4,2])
    C0557978 (UMLS CUI [4,3])
    C0201976 (UMLS CUI [5,1])
    C0445204 (UMLS CUI [5,2])
    Item Group
    C0680251 (UMLS CUI)
    contraindication to metoprolol
    Item
    contraindication to metoprolol including any of the following: significant bradycardia (heart rate < 50 beats per minute); second or third degree heart block without a pacemaker; asthma that has been active within the last decade; and history of chronic obstructive pulmonary disease (copd) with bronchospasm on pulmonary function tests.
    boolean
    C0428977 (UMLS CUI [1])
    C0264906 (UMLS CUI [2])
    C0151517 (UMLS CUI [3])
    C0004096 (UMLS CUI [4])
    C0024117 (UMLS CUI [5])
    beta-blocker usage
    Item
    clinical plan to use a beta-blocker preoperatively or during the first 30 postoperative days
    boolean
    C0001645 (UMLS CUI [1])
    hypersensitivity to beta-blocker
    Item
    prior adverse reaction to a beta-blocker
    boolean
    C0020517 (UMLS CUI [1,1])
    C0001645 (UMLS CUI [1,2])
    cabg
    Item
    coronary artery bypass graft (cabg) surgery with complete revascularization in the preceding 5 years and no evidence of cardiac ischemia since the cabg surgery
    boolean
    C0010055 (UMLS CUI [1,1])
    C0151744 (UMLS CUI [1,2])
    C0332197 (UMLS CUI [1,3])
    low risk surgery
    Item
    patients undergoing low risk surgical procedures (potential examples include transurethral procedures [transurethral prostatectomies (turps), stone baskets, etc.], ophthalmologic procedures under topical or regional anesthesia [cornea transplants, cataract surgery, etc.], and surgeries with limited physiological stresses [digital re-implantation, nerve repairs, etc.] )
    boolean
    C0543467 (UMLS CUI [1,1])
    C3538919 (UMLS CUI [1,2])
    concurrent use of verapamil
    Item
    concurrent use of verapamil
    boolean
    C0009429 (UMLS CUI [1,1])
    C0042523 (UMLS CUI [1,2])
    prior enrollment in this trial
    Item
    prior enrollment in this trial
    boolean
    C1516879 (UMLS CUI [1,1])
    C0332152 (UMLS CUI [1,2])
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