ID

28283

Description

The Northern-European Initiative on Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00883792

Link

https://clinicaltrials.gov/show/NCT00883792

Keywords

Versions (1)
  1. 1/2/18 1/2/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 2, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT00883792

English

Eligibility Colorectal Cancer NCT00883792

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
this study is a population-based randomised controlled trial, with randomisation of individuals age 55-64 years living in the screening areas directly from the population registries to either screening group or control group. eligible persons with the same home address will be randomised to the same group (household randomisation).
Description

Controlled Clinical Trial, Randomized | Age | Residence Screening Area | Screening Groups | Control Groups

Data type

boolean

Alias
UMLS CUI [1]
C0206035
UMLS CUI [2]
C0001779
UMLS CUI [3,1]
C0237096
UMLS CUI [3,2]
C1710032
UMLS CUI [3,3]
C0017446
UMLS CUI [4,1]
C1710032
UMLS CUI [4,2]
C0441833
UMLS CUI [5]
C0009932
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
individuals with previous colorectal surgery (resections, enterostomies)
Description

Colorectal Surgery | Excision | Enterostomy

Data type

boolean

Alias
UMLS CUI [1]
C2608114
UMLS CUI [2]
C0728940
UMLS CUI [3]
C0014370
individuals in need of long-lasting attention and nursing services (somatic or psychosocial, mental retardation).
Description

Nursing Services Somatic Long-term Patient need for | Nursing Services Psychosocial Long-term Patient need for | Mental Retardation

Data type

boolean

Alias
UMLS CUI [1,1]
C0028697
UMLS CUI [1,2]
C2986476
UMLS CUI [1,3]
C0443252
UMLS CUI [1,4]
C0686904
UMLS CUI [2,1]
C0028697
UMLS CUI [2,2]
C0542298
UMLS CUI [2,3]
C0443252
UMLS CUI [2,4]
C0686904
UMLS CUI [3]
C0025362
on-going cytotoxic treatment or radiotherapy for malignant disease
Description

Cytotoxic therapy Malignant disease | Therapeutic radiology procedure Malignant disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0677881
UMLS CUI [1,2]
C0442867
UMLS CUI [2,1]
C1522449
UMLS CUI [2,2]
C0442867
severe chronic (longer than trial duration) cardiac (nyha iii-iv)or lung disease
Description

Chronic heart disease Severe New York Heart Association Classification | Chronic lung disease Severe

Data type

boolean

Alias
UMLS CUI [1,1]
C1290386
UMLS CUI [1,2]
C0205082
UMLS CUI [1,3]
C1275491
UMLS CUI [2,1]
C0746102
UMLS CUI [2,2]
C0205082
lifelong anticoagulant therapy with warfarin
Description

Anticoagulation Therapy Lifelong | Warfarin Lifelong

Data type

boolean

Alias
UMLS CUI [1,1]
C0003281
UMLS CUI [1,2]
C4274169
UMLS CUI [2,1]
C0043031
UMLS CUI [2,2]
C4274169
a coronary event requiring hospitalization during the last 3 months
Description

Coronary disease Hospitalization Required

Data type

boolean

Alias
UMLS CUI [1,1]
C0010068
UMLS CUI [1,2]
C1708385
a cerebrovascular event during the last 3 months
Description

Cerebrovascular Disorder

Data type

boolean

Alias
UMLS CUI [1]
C0007820
resident abroad
Description

Residence Country foreign

Data type

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0454664
UMLS CUI [1,3]
C1517294
return of unopened letter of invitation and/or reminder (address unknown)
Description

Patient address unknown

Data type

boolean

Alias
UMLS CUI [1]
C0421464
message from neighbour/family/post office on death of screenee (not updated in population registry)
Description

Patient died

Data type

boolean

Alias
UMLS CUI [1]
C1306577
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Similar models

Eligibility Colorectal Cancer NCT00883792

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Controlled Clinical Trial, Randomized | Age | Residence Screening Area | Screening Groups | Control Groups
Item
this study is a population-based randomised controlled trial, with randomisation of individuals age 55-64 years living in the screening areas directly from the population registries to either screening group or control group. eligible persons with the same home address will be randomised to the same group (household randomisation).
boolean
C0206035 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0237096 (UMLS CUI [3,1])
C1710032 (UMLS CUI [3,2])
C0017446 (UMLS CUI [3,3])
C1710032 (UMLS CUI [4,1])
C0441833 (UMLS CUI [4,2])
C0009932 (UMLS CUI [5])
Item Group
C0680251 (UMLS CUI)
Colorectal Surgery | Excision | Enterostomy
Item
individuals with previous colorectal surgery (resections, enterostomies)
boolean
C2608114 (UMLS CUI [1])
C0728940 (UMLS CUI [2])
C0014370 (UMLS CUI [3])
Nursing Services Somatic Long-term Patient need for | Nursing Services Psychosocial Long-term Patient need for | Mental Retardation
Item
individuals in need of long-lasting attention and nursing services (somatic or psychosocial, mental retardation).
boolean
C0028697 (UMLS CUI [1,1])
C2986476 (UMLS CUI [1,2])
C0443252 (UMLS CUI [1,3])
C0686904 (UMLS CUI [1,4])
C0028697 (UMLS CUI [2,1])
C0542298 (UMLS CUI [2,2])
C0443252 (UMLS CUI [2,3])
C0686904 (UMLS CUI [2,4])
C0025362 (UMLS CUI [3])
Cytotoxic therapy Malignant disease | Therapeutic radiology procedure Malignant disease
Item
on-going cytotoxic treatment or radiotherapy for malignant disease
boolean
C0677881 (UMLS CUI [1,1])
C0442867 (UMLS CUI [1,2])
C1522449 (UMLS CUI [2,1])
C0442867 (UMLS CUI [2,2])
Chronic heart disease Severe New York Heart Association Classification | Chronic lung disease Severe
Item
severe chronic (longer than trial duration) cardiac (nyha iii-iv)or lung disease
boolean
C1290386 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,3])
C0746102 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Anticoagulation Therapy Lifelong | Warfarin Lifelong
Item
lifelong anticoagulant therapy with warfarin
boolean
C0003281 (UMLS CUI [1,1])
C4274169 (UMLS CUI [1,2])
C0043031 (UMLS CUI [2,1])
C4274169 (UMLS CUI [2,2])
Coronary disease Hospitalization Required
Item
a coronary event requiring hospitalization during the last 3 months
boolean
C0010068 (UMLS CUI [1,1])
C1708385 (UMLS CUI [1,2])
Cerebrovascular Disorder
Item
a cerebrovascular event during the last 3 months
boolean
C0007820 (UMLS CUI [1])
Residence Country foreign
Item
resident abroad
boolean
C0237096 (UMLS CUI [1,1])
C0454664 (UMLS CUI [1,2])
C1517294 (UMLS CUI [1,3])
Patient address unknown
Item
return of unopened letter of invitation and/or reminder (address unknown)
boolean
C0421464 (UMLS CUI [1])
Patient died
Item
message from neighbour/family/post office on death of screenee (not updated in population registry)
boolean
C1306577 (UMLS CUI [1])
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