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ID

18645

Description

The Use of Platelet Derived Growth Factors in Total Knee Arthroplasty, a Randomized Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00167895

Lien

https://clinicaltrials.gov/show/NCT00167895

Mots-clés

Versions (1)
  1. 14/11/2016 14/11/2016 -
Téléchargé le

14 novembre 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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    Eligibility Osteoarthritis NCT00167895

    Anglais

    Eligibility Osteoarthritis NCT00167895

    1 Formulaires  
    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693 (Inclusion)
    patients undergoing primary total knee arthroplasty for primary osteoarthritis
    Description

    Osteoarthritis Primary | Knee Replacement Arthroplasty Primary

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0029408 (Degenerative polyarthritis)
    SNOMED
    396275006
    LOINC
    LA17768-5
    UMLS CUI [1,2]
    C0205225 (Primary)
    SNOMED
    63161005
    LOINC
    LA21208-6
    UMLS CUI [2,1]
    C0086511 (Knee Replacement Arthroplasty (procedure))
    SNOMED
    609588000
    LOINC
    LA25611-7
    UMLS CUI [2,2]
    C0205225 (Primary)
    SNOMED
    63161005
    LOINC
    LA21208-6
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251 (Exclusion Criteria)
    coagulation disorder
    Description

    Blood Coagulation Disorder

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0005779 (Blood Coagulation Disorders)
    SNOMED
    64779008
    abnormal pre-operative levels of aptt, pt and/or thrombocytes
    Description

    Activated Partial Thromboplastin Time measurement Preoperative Abnormal | Prothrombin time assay Preoperative Abnormal | Platelet Count measurement Preoperative Abnormal

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0030605 (Activated Partial Thromboplastin Time measurement)
    SNOMED
    42525009
    UMLS CUI [1,2]
    C0445204 (Preoperative)
    SNOMED
    262068006
    LOINC
    LP91296-1
    UMLS CUI [1,3]
    C0205161 (Abnormal)
    SNOMED
    263654008
    LOINC
    LP28764-6
    UMLS CUI [2,1]
    C0033707 (Prothrombin time assay)
    SNOMED
    396451008
    UMLS CUI [2,2]
    C0445204 (Preoperative)
    SNOMED
    262068006
    LOINC
    LP91296-1
    UMLS CUI [2,3]
    C0205161 (Abnormal)
    SNOMED
    263654008
    LOINC
    LP28764-6
    UMLS CUI [3,1]
    C0032181 (Platelet Count measurement)
    SNOMED
    61928009
    UMLS CUI [3,2]
    C0445204 (Preoperative)
    SNOMED
    262068006
    LOINC
    LP91296-1
    UMLS CUI [3,3]
    C0205161 (Abnormal)
    SNOMED
    263654008
    LOINC
    LP28764-6
    homologous blood transfusion last 4 weeks
    Description

    Blood Transfusion Homologous

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0005841 (Blood Transfusion)
    SNOMED
    116859006
    LOINC
    LP32812-7
    UMLS CUI [1,2]
    C0301883 (Homologous state)
    SNOMED
    37505000
    coagulation disorder
    Description

    Blood Coagulation Disorder

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0005779 (Blood Coagulation Disorders)
    SNOMED
    64779008
    use of anticoagulation medication
    Description

    Anticoagulants

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0003280 (Anticoagulants)
    SNOMED
    81839001
    use of any iron supplements or erythropoietin at time of operation or during 1 week prior to operation
    Description

    Iron Supplement Perioperative Period | Erythropoietin Perioperative Period

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0721124 (Iron Supplement)
    SNOMED
    438641000124100
    UMLS CUI [1,2]
    C2712230 (Perioperative Period)
    UMLS CUI [2,1]
    C0014822 (Erythropoietin)
    SNOMED
    111167001
    LOINC
    LP15554-6
    UMLS CUI [2,2]
    C2712230 (Perioperative Period)
    primary bone tumor or metastatic bone disease
    Description

    Bone neoplasm Primary | Secondary malignant neoplasm of bone

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0005967 (Bone neoplasms)
    SNOMED
    115239009
    UMLS CUI [1,2]
    C0205225 (Primary)
    SNOMED
    63161005
    LOINC
    LA21208-6
    UMLS CUI [2]
    C0153690 (Secondary malignant neoplasm of bone)
    SNOMED
    94222008
    unable or unwilling to participate in follow-up
    Description

    Follow-up participation Unwilling

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C3274571 (Clinical Study Follow-up)
    UMLS CUI [1,2]
    C0679823 (Participation)
    UMLS CUI [1,3]
    C0558080 (Unwilling)
    SNOMED
    225465005
    unable to give informed consent
    Description

    Informed Consent Unable

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0021430 (Informed Consent)
    UMLS CUI [1,2]
    C1299582 (Unable)
    SNOMED
    371151008
    LOINC
    LA13868-7
    previous infection in knee
    Description

    knee; infection

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C1400580 (knee; infection)
    use of corticosteroids at time of operation or during 4 weeks prior to operation
    Description

    Adrenal Cortex Hormones Perioperative Period

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0001617 (Adrenal Cortex Hormones)
    SNOMED
    21568003
    LOINC
    LP20687-7
    UMLS CUI [1,2]
    C2712230 (Perioperative Period)
    any neuromuscular disorder
    Description

    Neuromuscular Disease

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0027868 (Neuromuscular Diseases)
    SNOMED
    257277002
    active infection or osteomyelitis
    Description

    Communicable Disease | Osteomyelitis

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0009450 (Communicable Diseases)
    SNOMED
    189822004
    UMLS CUI [2]
    C0029443 (Osteomyelitis)
    SNOMED
    60168000
    LOINC
    LP128775-6
    Retour au début de la page

    Similar models

    Eligibility Osteoarthritis NCT00167895

    1 Formulaires
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Osteoarthritis Primary | Knee Replacement Arthroplasty Primary
    Item
    patients undergoing primary total knee arthroplasty for primary osteoarthritis
    boolean
    C0029408 (UMLS CUI [1,1])
    C0205225 (UMLS CUI [1,2])
    C0086511 (UMLS CUI [2,1])
    C0205225 (UMLS CUI [2,2])
    Item Group
    C0680251 (UMLS CUI)
    Blood Coagulation Disorder
    Item
    coagulation disorder
    boolean
    C0005779 (UMLS CUI [1])
    Activated Partial Thromboplastin Time measurement Preoperative Abnormal | Prothrombin time assay Preoperative Abnormal | Platelet Count measurement Preoperative Abnormal
    Item
    abnormal pre-operative levels of aptt, pt and/or thrombocytes
    boolean
    C0030605 (UMLS CUI [1,1])
    C0445204 (UMLS CUI [1,2])
    C0205161 (UMLS CUI [1,3])
    C0033707 (UMLS CUI [2,1])
    C0445204 (UMLS CUI [2,2])
    C0205161 (UMLS CUI [2,3])
    C0032181 (UMLS CUI [3,1])
    C0445204 (UMLS CUI [3,2])
    C0205161 (UMLS CUI [3,3])
    Blood Transfusion Homologous
    Item
    homologous blood transfusion last 4 weeks
    boolean
    C0005841 (UMLS CUI [1,1])
    C0301883 (UMLS CUI [1,2])
    Blood Coagulation Disorder
    Item
    coagulation disorder
    boolean
    C0005779 (UMLS CUI [1])
    Anticoagulants
    Item
    use of anticoagulation medication
    boolean
    C0003280 (UMLS CUI [1])
    Iron Supplement Perioperative Period | Erythropoietin Perioperative Period
    Item
    use of any iron supplements or erythropoietin at time of operation or during 1 week prior to operation
    boolean
    C0721124 (UMLS CUI [1,1])
    C2712230 (UMLS CUI [1,2])
    C0014822 (UMLS CUI [2,1])
    C2712230 (UMLS CUI [2,2])
    Bone neoplasm Primary | Secondary malignant neoplasm of bone
    Item
    primary bone tumor or metastatic bone disease
    boolean
    C0005967 (UMLS CUI [1,1])
    C0205225 (UMLS CUI [1,2])
    C0153690 (UMLS CUI [2])
    Follow-up participation Unwilling
    Item
    unable or unwilling to participate in follow-up
    boolean
    C3274571 (UMLS CUI [1,1])
    C0679823 (UMLS CUI [1,2])
    C0558080 (UMLS CUI [1,3])
    Informed Consent Unable
    Item
    unable to give informed consent
    boolean
    C0021430 (UMLS CUI [1,1])
    C1299582 (UMLS CUI [1,2])
    knee; infection
    Item
    previous infection in knee
    boolean
    C1400580 (UMLS CUI [1])
    Adrenal Cortex Hormones Perioperative Period
    Item
    use of corticosteroids at time of operation or during 4 weeks prior to operation
    boolean
    C0001617 (UMLS CUI [1,1])
    C2712230 (UMLS CUI [1,2])
    Neuromuscular Disease
    Item
    any neuromuscular disorder
    boolean
    C0027868 (UMLS CUI [1])
    Communicable Disease | Osteomyelitis
    Item
    active infection or osteomyelitis
    boolean
    C0009450 (UMLS CUI [1])
    C0029443 (UMLS CUI [2])
    Retour au début de la page 

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