Eligibility Localized, Primary Osteoarthritis NCT02444299

Inclusion Criteria
Descrizione

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 ;
Descrizione

ID.1

Tipo di dati

boolean

with a functional rotator cuff ;
Descrizione

ID.2

Tipo di dati

boolean

has clinical and radiographic follow-up data available ;
Descrizione

ID.3

Tipo di dati

boolean

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

ID.4

Tipo di dati

boolean

Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient with proximal humeral fracture,
Descrizione

ID.5

Tipo di dati

boolean

previous history of infection,
Descrizione

ID.6

Tipo di dati

boolean

rotator cuff tear, cuff tear arthropathy,
Descrizione

ID.7

Tipo di dati

boolean

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

ID.8

Tipo di dati

boolean

nerve palsy,
Descrizione

ID.9

Tipo di dati

boolean

revision arthroplasty.
Descrizione

ID.10

Tipo di dati

boolean

Similar models

Eligibility Localized, Primary Osteoarthritis NCT02444299

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
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