ID

19222

Beschrijving

A Multi-centre Study to Assess the Long-term Performance of the Summit™ Hip in Primary Total Hip Replacement; ODM derived from: https://clinicaltrials.gov/show/NCT00208390

Link

https://clinicaltrials.gov/show/NCT00208390

Trefwoorden

Versies (2)
  1. 11-12-16 11-12-16 -
  2. 13-12-16 13-12-16 -
Geüploaded op

13 december 2016

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00208390

Engels

Eligibility Rheumatoid Arthritis NCT00208390

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
i) male or female subjects, aged between 18 and 70 years (inclusive).
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ii) subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
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.
Beschrijving

Comprehension Study Protocol | Protocol Compliance | Postoperative follow-up visit Compliance behavior

Datatype

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C0525058
UMLS CUI [3,1]
C2585426
UMLS CUI [3,2]
C1321605
iv) subjects who require primary total hip replacement and are considered suitable for a cementless femoral stem.
Beschrijving

Total Hip Replacement Primary Patient need for | Femoral Stem Component Bone Cement Lack

Datatype

boolean

Alias
UMLS CUI [1,1]
C0040508
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C0686904
UMLS CUI [2,1]
C1961410
UMLS CUI [2,2]
C0005934
UMLS CUI [2,3]
C0332268
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
i) subjects who, in the opinion of the investigator, have an existing condition that would compromise their participation and follow-up in this study.
Beschrijving

Condition Affecting Study Subject Participation Status | Condition Affecting Clinical Study Follow-up

Datatype

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C2348568
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C3274571
ii) subjects who have previously undergone a hemi-arthroplasty or total hip arthroplasty.
Beschrijving

Hemiarthroplasty | Total Hip Replacement

Datatype

boolean

Alias
UMLS CUI [1]
C0744743
UMLS CUI [2]
C0040508
iii) women who are pregnant.
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
iv) subjects who are known drug or alcohol abusers or with psychological disorders that could effect follow-up care or treatment outcomes.
Beschrijving

Substance Use Disorders | Mental disorders Affecting Follow-Up Care | Mental disorders Affecting Treatment outcome

Datatype

boolean

Alias
UMLS CUI [1]
C0038586
UMLS CUI [2,1]
C0004936
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C3899107
UMLS CUI [3,1]
C0004936
UMLS CUI [3,2]
C0392760
UMLS CUI [3,3]
C0085415
v) subjects who have participated in a clinical study with an investigational product in the last 12 months.
Beschrijving

Study Subject Participation Status | Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
vi) subjects who are currently involved in any injury litigation claims.
Beschrijving

Litigation Involvement with

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079706
UMLS CUI [1,2]
C1314939
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Similar models

Eligibility Rheumatoid Arthritis NCT00208390

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
i) male or female subjects, aged between 18 and 70 years (inclusive).
boolean
C0001779 (UMLS CUI [1])
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])
Comprehension Study Protocol | Protocol Compliance | Postoperative follow-up visit Compliance behavior
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
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
C2585426 (UMLS CUI [3,1])
C1321605 (UMLS CUI [3,2])
Total Hip Replacement Primary Patient need for | Femoral Stem Component Bone Cement Lack
Item
iv) subjects who require primary total hip replacement and are considered suitable for a cementless femoral stem.
boolean
C0040508 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0686904 (UMLS CUI [1,3])
C1961410 (UMLS CUI [2,1])
C0005934 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
Item Group
C0680251 (UMLS CUI)
Condition Affecting Study Subject Participation Status | Condition Affecting Clinical Study Follow-up
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
C0348080 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C3274571 (UMLS CUI [2,3])
Hemiarthroplasty | Total Hip Replacement
Item
ii) subjects who have previously undergone a hemi-arthroplasty or total hip arthroplasty.
boolean
C0744743 (UMLS CUI [1])
C0040508 (UMLS CUI [2])
Pregnancy
Item
iii) women who are pregnant.
boolean
C0032961 (UMLS CUI [1])
Substance Use Disorders | Mental disorders Affecting Follow-Up Care | Mental disorders Affecting Treatment outcome
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 [2,1])
C0392760 (UMLS CUI [2,2])
C3899107 (UMLS CUI [2,3])
C0004936 (UMLS CUI [3,1])
C0392760 (UMLS CUI [3,2])
C0085415 (UMLS CUI [3,3])
Study Subject Participation Status | Investigational New Drugs
Item
v) subjects who have participated in a clinical study with an investigational product in the last 12 months.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
Litigation Involvement with
Item
vi) subjects who are currently involved in any injury litigation claims.
boolean
C0079706 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
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