ID

34388

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT02444299

Trefwoorden

  1. 17/01/2019 17/01/2019 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 de janeiro de 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

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Eligibility Localized, Primary Osteoarthritis NCT02444299

Eligibility Localized, Primary Osteoarthritis NCT02444299

Inclusion Criteria
Beschrijving

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 ;
Beschrijving

ID.1

Datatype

boolean

with a functional rotator cuff ;
Beschrijving

ID.2

Datatype

boolean

has clinical and radiographic follow-up data available ;
Beschrijving

ID.3

Datatype

boolean

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

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient with proximal humeral fracture,
Beschrijving

ID.5

Datatype

boolean

previous history of infection,
Beschrijving

ID.6

Datatype

boolean

rotator cuff tear, cuff tear arthropathy,
Beschrijving

ID.7

Datatype

boolean

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

ID.8

Datatype

boolean

nerve palsy,
Beschrijving

ID.9

Datatype

boolean

revision arthroplasty.
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Localized, Primary Osteoarthritis NCT02444299

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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