ID

34009

Beschrijving

Prevalence Study of Gastrointestinal Risk Factors in Patients With Osteoarthritis (OA), Rheumatoid Arthritis (RA) and Ankylosing Spondylitis (AS).; ODM derived from: https://clinicaltrials.gov/show/NCT01577563

Link

https://clinicaltrials.gov/show/NCT01577563

Trefwoorden

  1. 10-01-19 10-01-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

10 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Osteoarthritis (OA) NCT01577563

Eligibility Osteoarthritis (OA) NCT01577563

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
provision of subject informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
female and/or male, aged > 21 years.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
patients diagnosis with ra (acr 1987 or acr/eular 2010 criteria), oa (acr 1986, 1990 and 1991 criteria) or as (new york 1984 criteria or essg 2002 criteria) (documented in the medical record).
Beschrijving

Rheumatoid Arthritis | Osteoarthritis | Ankylosing spondylitis

Datatype

boolean

Alias
UMLS CUI [1]
C0003873
UMLS CUI [2]
C0029408
UMLS CUI [3]
C0038013
patients receiving at least one dose of nsaids.
Beschrijving

NSAIDs Dose Quantity

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003211
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1265611
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
participation in any interventional study involving investigational drugs.
Beschrijving

Study Subject Participation Status | Interventional Study Involving Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C3274035
UMLS CUI [2,2]
C1314939
UMLS CUI [2,3]
C0013230
patient refuses to fill in the study questionnaires.
Beschrijving

Clinical Trial Subject Questionnaire Completion Refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C3890411
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C1705116
pregnant or breastfeeding women.
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients with active neoplastic disease in the last 5 years, except basal-cell carcinoma.
Beschrijving

Neoplastic disease | Exception Basal cell carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C1882062
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0007117

Similar models

Eligibility Osteoarthritis (OA) NCT01577563

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
provision of subject informed consent.
boolean
C0021430 (UMLS CUI [1])
Age
Item
female and/or male, aged > 21 years.
boolean
C0001779 (UMLS CUI [1])
Rheumatoid Arthritis | Osteoarthritis | Ankylosing spondylitis
Item
patients diagnosis with ra (acr 1987 or acr/eular 2010 criteria), oa (acr 1986, 1990 and 1991 criteria) or as (new york 1984 criteria or essg 2002 criteria) (documented in the medical record).
boolean
C0003873 (UMLS CUI [1])
C0029408 (UMLS CUI [2])
C0038013 (UMLS CUI [3])
NSAIDs Dose Quantity
Item
patients receiving at least one dose of nsaids.
boolean
C0003211 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status | Interventional Study Involving Investigational New Drugs
Item
participation in any interventional study involving investigational drugs.
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C0013230 (UMLS CUI [2,3])
Clinical Trial Subject Questionnaire Completion Refused
Item
patient refuses to fill in the study questionnaires.
boolean
C3890411 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1705116 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Neoplastic disease | Exception Basal cell carcinoma
Item
patients with active neoplastic disease in the last 5 years, except basal-cell carcinoma.
boolean
C1882062 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0007117 (UMLS CUI [2,2])

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