Information:
Fel:
ID
22273
Beskrivning
A Two Centre Study to Assess the Stability and Long-term Performance of the C-Stem™ AMT in a Total Primary Hip Replacement; ODM derived from: https://clinicaltrials.gov/show/NCT00872573
Länk
https://clinicaltrials.gov/show/NCT00872573
Nyckelord
Versioner (1)
- 2017-05-28 2017-05-28 -
Uppladdad den
28 maj 2017
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00872573
Eligibility Rheumatoid Arthritis NCT00872573
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00872573
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
gender, age
Item
i) male or female subjects, aged between 60 and 80 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
Item
iv) subjects undergoing primary total hip replacement that are considered suitable for a cemented femoral stem and metal femoral head and an all polyethylene acetabular cup.
boolean
C0040508 (UMLS CUI [1])
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])
simultaneous bilateral hip replacement
Item
iii) subjects undergoing simultaneous bilateral hip replacements.
boolean
C0040508 (UMLS CUI [1,1])
C0238767 (UMLS CUI [1,2])
C0521115 (UMLS CUI [1,3])
C0238767 (UMLS CUI [1,2])
C0521115 (UMLS CUI [1,3])
contralateral hip replacement
Item
iv) subjects with a contralateral hip replacement, which 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])
pregnancy
Item
v) women who are pregnant.
boolean
C0032961 (UMLS CUI [1])
substance abuse, psychological disorders
Item
vi) subjects who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.
boolean
C0038586 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0004936 (UMLS CUI [2])
study participation, investigational product
Item
vii) 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 litigation claims
Item
viii) 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])