ID

18605

Beschrijving

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

Trefwoorden

  1. 12-11-16 12-11-16 -
Geüploaded op

12 november 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Osteoarthritis NCT00116038

Eligibility Osteoarthritis NCT00116038

Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Coxitis Primary

Datatype

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.
Beschrijving

Bone Density Sufficient Related Uncemented component fixation Femoral

Datatype

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.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

Neuromuscular Disease Leg Affected | Vascular Disease Leg Affected

Datatype

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.
Beschrijving

Patient Inappropriate Uncemented component fixation acetabulum | Operative Surgical Procedure

Datatype

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.
Beschrijving

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

Datatype

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.
Beschrijving

sequelae of; fracture

Datatype

boolean

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

Gender Childbearing Potential

Datatype

boolean

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

Dysplasia Hip Joint

Datatype

boolean

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

sequelae Due to Disorder of hip joint Childhood

Datatype

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)
Datatype
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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