ID

34388

Descripción

Aequalis Resurfacing Head Study; ODM derived from: https://clinicaltrials.gov/show/NCT02444299

Link

https://clinicaltrials.gov/show/NCT02444299

Palabras clave

  1. 17/1/19 17/1/19 -
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

17 de enero de 2019

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Localized, Primary Osteoarthritis NCT02444299

Eligibility Localized, Primary Osteoarthritis NCT02444299

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient has received an aequalis® resurfacing head implant as per the manufacturer's instructions (including the recommended indication): degenerative indication such as primary osteoarthritis, secondary osteoarthritis (post-traumatic post instability), avascular osteonecrosis of the humeral head ;
Descripción

ID.1

Tipo de datos

boolean

with a functional rotator cuff ;
Descripción

ID.2

Tipo de datos

boolean

has clinical and radiographic follow-up data available ;
Descripción

ID.3

Tipo de datos

boolean

is informed about the study and has provided informed consent as applicable.
Descripción

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient with proximal humeral fracture,
Descripción

ID.5

Tipo de datos

boolean

previous history of infection,
Descripción

ID.6

Tipo de datos

boolean

rotator cuff tear, cuff tear arthropathy,
Descripción

ID.7

Tipo de datos

boolean

significant bone loss of the glenoid (more than 25% of the articular surface),
Descripción

ID.8

Tipo de datos

boolean

nerve palsy,
Descripción

ID.9

Tipo de datos

boolean

revision arthroplasty.
Descripción

ID.10

Tipo de datos

boolean

Similar models

Eligibility Localized, Primary Osteoarthritis NCT02444299

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patient has received an aequalis® resurfacing head implant as per the manufacturer's instructions (including the recommended indication): degenerative indication such as primary osteoarthritis, secondary osteoarthritis (post-traumatic post instability), avascular osteonecrosis of the humeral head ;
boolean
ID.2
Item
with a functional rotator cuff ;
boolean
ID.3
Item
has clinical and radiographic follow-up data available ;
boolean
ID.4
Item
is informed about the study and has provided informed consent as applicable.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
patient with proximal humeral fracture,
boolean
ID.6
Item
previous history of infection,
boolean
ID.7
Item
rotator cuff tear, cuff tear arthropathy,
boolean
ID.8
Item
significant bone loss of the glenoid (more than 25% of the articular surface),
boolean
ID.9
Item
nerve palsy,
boolean
ID.10
Item
revision arthroplasty.
boolean

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