ID

34388

Description

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

Lien

https://clinicaltrials.gov/show/NCT02444299

Mots-clés

  1. 17/01/2019 17/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

17 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Localized, Primary Osteoarthritis NCT02444299

Eligibility Localized, Primary Osteoarthritis NCT02444299

Inclusion Criteria
Description

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 ;
Description

ID.1

Type de données

boolean

with a functional rotator cuff ;
Description

ID.2

Type de données

boolean

has clinical and radiographic follow-up data available ;
Description

ID.3

Type de données

boolean

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

ID.4

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient with proximal humeral fracture,
Description

ID.5

Type de données

boolean

previous history of infection,
Description

ID.6

Type de données

boolean

rotator cuff tear, cuff tear arthropathy,
Description

ID.7

Type de données

boolean

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

ID.8

Type de données

boolean

nerve palsy,
Description

ID.9

Type de données

boolean

revision arthroplasty.
Description

ID.10

Type de données

boolean

Similar models

Eligibility Localized, Primary Osteoarthritis NCT02444299

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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