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

Link

https://clinicaltrials.gov/show/NCT00167895

Keywords

Versions (1)
  1. 11/14/16 11/14/16 -
Uploaded on

November 14, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Osteoarthritis NCT00167895

English

Eligibility Osteoarthritis NCT00167895

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

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

Osteoarthritis Primary | Knee Replacement Arthroplasty Primary

Data type

boolean

Alias
UMLS CUI [1,1]
C0029408
UMLS CUI [1,2]
C0205225
UMLS CUI [2,1]
C0086511
UMLS CUI [2,2]
C0205225
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
coagulation disorder
Description

Blood Coagulation Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0005779
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

Data type

boolean

Alias
UMLS CUI [1,1]
C0030605
UMLS CUI [1,2]
C0445204
UMLS CUI [1,3]
C0205161
UMLS CUI [2,1]
C0033707
UMLS CUI [2,2]
C0445204
UMLS CUI [2,3]
C0205161
UMLS CUI [3,1]
C0032181
UMLS CUI [3,2]
C0445204
UMLS CUI [3,3]
C0205161
homologous blood transfusion last 4 weeks
Description

Blood Transfusion Homologous

Data type

boolean

Alias
UMLS CUI [1,1]
C0005841
UMLS CUI [1,2]
C0301883
coagulation disorder
Description

Blood Coagulation Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0005779
use of anticoagulation medication
Description

Anticoagulants

Data type

boolean

Alias
UMLS CUI [1]
C0003280
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

Data type

boolean

Alias
UMLS CUI [1,1]
C0721124
UMLS CUI [1,2]
C2712230
UMLS CUI [2,1]
C0014822
UMLS CUI [2,2]
C2712230
primary bone tumor or metastatic bone disease
Description

Bone neoplasm Primary | Secondary malignant neoplasm of bone

Data type

boolean

Alias
UMLS CUI [1,1]
C0005967
UMLS CUI [1,2]
C0205225
UMLS CUI [2]
C0153690
unable or unwilling to participate in follow-up
Description

Follow-up participation Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0679823
UMLS CUI [1,3]
C0558080
unable to give informed consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
previous infection in knee
Description

knee; infection

Data type

boolean

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

Adrenal Cortex Hormones Perioperative Period

Data type

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C2712230
any neuromuscular disorder
Description

Neuromuscular Disease

Data type

boolean

Alias
UMLS CUI [1]
C0027868
active infection or osteomyelitis
Description

Communicable Disease | Osteomyelitis

Data type

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0029443
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Similar models

Eligibility Osteoarthritis NCT00167895

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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])
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