ID

18605

Description

A Comparison of Two Metal Surface Finishes on Femoral Components in Hip Arthroplasty; ODM derived from: https://clinicaltrials.gov/show/NCT00116038

Link

https://clinicaltrials.gov/show/NCT00116038

Keywords

  1. 11/12/16 11/12/16 -
Uploaded on

November 12, 2016

DOI

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License

Creative Commons BY 4.0

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Eligibility Osteoarthritis NCT00116038

Eligibility Osteoarthritis NCT00116038

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with primary arthritis in the hip.
Description

Coxitis Primary

Data type

boolean

Alias
UMLS CUI [1,1]
C0263776
UMLS CUI [1,2]
C0205225
patients with sufficient bone density to allow uncemented implantation of a femoral component.
Description

Bone Density Sufficient Related Uncemented component fixation Femoral

Data type

boolean

Alias
UMLS CUI [1,1]
C0005938
UMLS CUI [1,2]
C0205410
UMLS CUI [1,3]
C0439849
UMLS CUI [1,4]
C0582264
UMLS CUI [1,5]
C0015811
informed patient consent in writing.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with neuromuscular or vascular disease in the affected leg.
Description

Neuromuscular Disease Leg Affected | Vascular Disease Leg Affected

Data type

boolean

Alias
UMLS CUI [1,1]
C0027868
UMLS CUI [1,2]
C1140621
UMLS CUI [1,3]
C0392760
UMLS CUI [2,1]
C0042373
UMLS CUI [2,2]
C1140621
UMLS CUI [2,3]
C0392760
patients found upon operation to be unsuited for uncemented acetabulum component.
Description

Patient Inappropriate Uncemented component fixation acetabulum | Operative Surgical Procedure

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548788
UMLS CUI [1,3]
C0582264
UMLS CUI [1,4]
C0000962
UMLS CUI [2]
C0543467
patients who regularly take non-steroid anti-inflammatory drugs (nsaid) and cannot interrupt intake for the postoperative phase of the study.
Description

Non-Steroidal Anti-Inflammatory Agents Intake Regular | Intake Discontinue Unable Postoperative Period

Data type

boolean

Alias
UMLS CUI [1,1]
C0003211
UMLS CUI [1,2]
C1512806
UMLS CUI [1,3]
C0205272
UMLS CUI [2,1]
C1512806
UMLS CUI [2,2]
C1444662
UMLS CUI [2,3]
C1299582
UMLS CUI [2,4]
C0032790
patients with fracture sequelae.
Description

sequelae of; fracture

Data type

boolean

Alias
UMLS CUI [1]
C1397722
female patients of childbearing capacity.
Description

Gender Childbearing Potential

Data type

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C3831118
hip joint dysplasia.
Description

Dysplasia Hip Joint

Data type

boolean

Alias
UMLS CUI [1,1]
C0334044
UMLS CUI [1,2]
C0019558
sequelae to previous hip joint disorder in childhood.
Description

sequelae Due to Disorder of hip joint Childhood

Data type

boolean

Alias
UMLS CUI [1,1]
C0243088
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C1998415
UMLS CUI [1,4]
C0231335

Similar models

Eligibility Osteoarthritis NCT00116038

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Coxitis Primary
Item
patients with primary arthritis in the hip.
boolean
C0263776 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
Bone Density Sufficient Related Uncemented component fixation Femoral
Item
patients with sufficient bone density to allow uncemented implantation of a femoral component.
boolean
C0005938 (UMLS CUI [1,1])
C0205410 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C0582264 (UMLS CUI [1,4])
C0015811 (UMLS CUI [1,5])
Informed Consent
Item
informed patient consent in writing.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Neuromuscular Disease Leg Affected | Vascular Disease Leg Affected
Item
patients with neuromuscular or vascular disease in the affected leg.
boolean
C0027868 (UMLS CUI [1,1])
C1140621 (UMLS CUI [1,2])
C0392760 (UMLS CUI [1,3])
C0042373 (UMLS CUI [2,1])
C1140621 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
Patient Inappropriate Uncemented component fixation acetabulum | Operative Surgical Procedure
Item
patients found upon operation to be unsuited for uncemented acetabulum component.
boolean
C0030705 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0582264 (UMLS CUI [1,3])
C0000962 (UMLS CUI [1,4])
C0543467 (UMLS CUI [2])
Non-Steroidal Anti-Inflammatory Agents Intake Regular | Intake Discontinue Unable Postoperative Period
Item
patients who regularly take non-steroid anti-inflammatory drugs (nsaid) and cannot interrupt intake for the postoperative phase of the study.
boolean
C0003211 (UMLS CUI [1,1])
C1512806 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,3])
C1512806 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
C0032790 (UMLS CUI [2,4])
sequelae of; fracture
Item
patients with fracture sequelae.
boolean
C1397722 (UMLS CUI [1])
Gender Childbearing Potential
Item
female patients of childbearing capacity.
boolean
C0079399 (UMLS CUI [1,1])
C3831118 (UMLS CUI [1,2])
Dysplasia Hip Joint
Item
hip joint dysplasia.
boolean
C0334044 (UMLS CUI [1,1])
C0019558 (UMLS CUI [1,2])
sequelae Due to Disorder of hip joint Childhood
Item
sequelae to previous hip joint disorder in childhood.
boolean
C0243088 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C1998415 (UMLS CUI [1,3])
C0231335 (UMLS CUI [1,4])

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