ID

34009

Description

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

Lien

https://clinicaltrials.gov/show/NCT01577563

Mots-clés

  1. 10/01/2019 10/01/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

10 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Osteoarthritis (OA) NCT01577563

Eligibility Osteoarthritis (OA) NCT01577563

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
provision of subject informed consent.
Description

Informed Consent

Type de données

boolean

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

Age

Type de données

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).
Description

Rheumatoid Arthritis | Osteoarthritis | Ankylosing spondylitis

Type de données

boolean

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

NSAIDs Dose Quantity

Type de données

boolean

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

Exclusion Criteria

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

Study Subject Participation Status | Interventional Study Involving Investigational New Drugs

Type de données

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.
Description

Clinical Trial Subject Questionnaire Completion Refused

Type de données

boolean

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

Pregnancy | Breast Feeding

Type de données

boolean

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

Neoplastic disease | Exception Basal cell carcinoma

Type de données

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)
Type de données
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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