Informatie:
Fout:
ID
22269
Beschrijving
A Single Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-ceramic Bearing in Primary Total Hip Replacement; ODM derived from: https://clinicaltrials.gov/show/NCT00872222
Link
https://clinicaltrials.gov/show/NCT00872222
Trefwoorden
Versies (1)
- 28-05-17 28-05-17 -
Geüploaded op
28 mei 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00872222
Eligibility Rheumatoid Arthritis NCT00872222
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00872222
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
gender, age
Item
i) male or female subjects, aged between 18 and 70 years inclusive.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
informed consent
Item
ii) subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained.
boolean
C0021430 (UMLS CUI [1])
compliance
Item
iii) subjects who, in the opinion of the investigator, are able to understand this investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.
boolean
C1321605 (UMLS CUI [1])
total hip replacement, cementless acetabular components
Item
iv) subjects undergoing primary total hip replacement who are suitable for cementless acetabular components.
boolean
C0040508 (UMLS CUI [1,1])
C0182473 (UMLS CUI [1,2])
C0005934 (UMLS CUI [1,3])
C0182473 (UMLS CUI [1,2])
C0005934 (UMLS CUI [1,3])
comorbidity
Item
i) subjects who, in the opinion of the investigator, have an existing condition that would compromise their participation and follow-up in this study.
boolean
C0009488 (UMLS CUI [1])
revision hip replacement
Item
ii) subjects undergoing revision hip replacement.
boolean
C0186201 (UMLS CUI [1])
pregnancy
Item
iii) women who are pregnant.
boolean
C0032961 (UMLS CUI [1])
substance abuse, psychological disorders
Item
iv) subjects who are known drug or alcohol abusers or with psychological disorders that could effect follow-up care or treatment outcomes.
boolean
C0038586 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0004936 (UMLS CUI [2])
study participation, investigational product
Item
v) subjects who have participated in a clinical study with an investigational product in the last 12 months.
boolean
C2348568 (UMLS CUI [1,1])
C3898691 (UMLS CUI [1,2])
C3898691 (UMLS CUI [1,2])
injury ligitation claims
Item
vi) subjects who are currently involved in any injury litigation claims.
boolean
C3263723 (UMLS CUI [1,1])
C0079706 (UMLS CUI [1,2])
C0021677 (UMLS CUI [1,3])
C0079706 (UMLS CUI [1,2])
C0021677 (UMLS CUI [1,3])
simultaneous bilateral hip operation
Item
vii) subjects undergoing a simultaneous bilateral hip operation.
boolean
C0596706 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
C0521115 (UMLS CUI [1,3])
C0238767 (UMLS CUI [1,2])
C0521115 (UMLS CUI [1,3])
investigation participation with contralateral hip
Item
viii) subjects undergoing the second stage of a staged bilateral for whom the contralateral hip is part of this clinical investigation.
boolean
C2348568 (UMLS CUI [1,1])
C0019552 (UMLS CUI [1,2])
C0441988 (UMLS CUI [1,3])
C0019552 (UMLS CUI [1,2])
C0441988 (UMLS CUI [1,3])
contralateral hip replacement
Item
ix) subjects undergoing the second stage of a staged bilateral for whom the contralateral hip was implanted less than six months previously or is not performing satisfactorily
boolean
C0040508 (UMLS CUI [1,1])
C0441988 (UMLS CUI [1,2])
C0441988 (UMLS CUI [1,2])