ID

14183

Description

Alzheimer's Disease Anti-Inflammatory Prevention Trial (ADAPT); ODM derived from: https://clinicaltrials.gov/show/NCT00007189

Lien

https://clinicaltrials.gov/show/NCT00007189

Mots-clés

  1. 03/04/2016 03/04/2016 -
Téléchargé le

3 avril 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Alzheimer Disease NCT00007189

Eligibility Alzheimer Disease NCT00007189

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 70 years or older.
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
family history of parent, brother, or sister who has, or had, serious age-related memory loss, senility, dementia, or alzheimer's disease.
Description

family history dementia alzheimers disease senility

Type de données

boolean

Alias
UMLS CUI [1,1]
C0241889
UMLS CUI [1,2]
C0497327
UMLS CUI [1,3]
C0002395
UMLS CUI [1,4]
C0231337
study partner available to provide information on the cognitive status of the participant and to assist with monitoring of trial medications, if needed.
Description

cognitive status

Type de données

boolean

Alias
UMLS CUI [1]
C0945985
sufficient fluency in written and spoken english to participate in study visits and neuropsychological testing.
Description

english speaking; neuropsychological testing

Type de données

boolean

Alias
UMLS CUI [1]
C0376245
UMLS CUI [2]
C0027902
willingness to limit use of the following for the duration of the study: vitamin e (at doses greater than 400 iu per day), non-aspirin nsaids, histamine h2 receptor antagonists (tagamet, for example), corticosteroids, anti-inflammatory or analgesic doses of aspirin (greater than 81 mg per day), ginkgo biloba extracts
Description

vitamin e; nsaid; histamine h2 receptor antagonists; corticosteroids; aspirin; Ginkgo biloba extract

Type de données

boolean

Alias
UMLS CUI [1]
C0042874
UMLS CUI [2]
C0003211
UMLS CUI [3]
C0019593
UMLS CUI [4]
C0001617
UMLS CUI [5]
C0004057
UMLS CUI [6]
C0772125
ability and intention to participate in regular study visits, in the opinion of the study physician.
Description

compliance behaviour

Type de données

boolean

Alias
UMLS CUI [1]
C1321605
provision of informed consent.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of peptic ulcer disease with bleeding or obstruction.
Description

peptic ulcer disease

Type de données

boolean

Alias
UMLS CUI [1]
C0030920
clinically significant liver or kidney disease.
Description

liver disease; kidney disease

Type de données

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0022658
history of hypersensitivity to aspirin, ibuprofen, celecoxib, naproxen, or other nsaids.
Description

hypersensitivity aspirin ibuprofen nsaids

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0004057
UMLS CUI [1,3]
C0020740
UMLS CUI [1,4]
C0003211
use of anti-coagulant medication.
Description

anti-coagulant

Type de données

boolean

Alias
UMLS CUI [1]
C0003280
cognitive impairment or dementia.
Description

cognitive impairment; dementia

Type de données

boolean

Alias
UMLS CUI [1]
C1839000
UMLS CUI [2]
C0497327
current alcohol abuse or dependence
Description

alcohol abuse

Type de données

boolean

Alias
UMLS CUI [1]
C0085762

Similar models

Eligibility Alzheimer Disease NCT00007189

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
aged 70 years or older.
boolean
C0001779 (UMLS CUI [1])
family history dementia alzheimers disease senility
Item
family history of parent, brother, or sister who has, or had, serious age-related memory loss, senility, dementia, or alzheimer's disease.
boolean
C0241889 (UMLS CUI [1,1])
C0497327 (UMLS CUI [1,2])
C0002395 (UMLS CUI [1,3])
C0231337 (UMLS CUI [1,4])
cognitive status
Item
study partner available to provide information on the cognitive status of the participant and to assist with monitoring of trial medications, if needed.
boolean
C0945985 (UMLS CUI [1])
english speaking; neuropsychological testing
Item
sufficient fluency in written and spoken english to participate in study visits and neuropsychological testing.
boolean
C0376245 (UMLS CUI [1])
C0027902 (UMLS CUI [2])
vitamin e; nsaid; histamine h2 receptor antagonists; corticosteroids; aspirin; Ginkgo biloba extract
Item
willingness to limit use of the following for the duration of the study: vitamin e (at doses greater than 400 iu per day), non-aspirin nsaids, histamine h2 receptor antagonists (tagamet, for example), corticosteroids, anti-inflammatory or analgesic doses of aspirin (greater than 81 mg per day), ginkgo biloba extracts
boolean
C0042874 (UMLS CUI [1])
C0003211 (UMLS CUI [2])
C0019593 (UMLS CUI [3])
C0001617 (UMLS CUI [4])
C0004057 (UMLS CUI [5])
C0772125 (UMLS CUI [6])
compliance behaviour
Item
ability and intention to participate in regular study visits, in the opinion of the study physician.
boolean
C1321605 (UMLS CUI [1])
informed consent
Item
provision of informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
peptic ulcer disease
Item
history of peptic ulcer disease with bleeding or obstruction.
boolean
C0030920 (UMLS CUI [1])
liver disease; kidney disease
Item
clinically significant liver or kidney disease.
boolean
C0023895 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
hypersensitivity aspirin ibuprofen nsaids
Item
history of hypersensitivity to aspirin, ibuprofen, celecoxib, naproxen, or other nsaids.
boolean
C0020517 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C0020740 (UMLS CUI [1,3])
C0003211 (UMLS CUI [1,4])
anti-coagulant
Item
use of anti-coagulant medication.
boolean
C0003280 (UMLS CUI [1])
cognitive impairment; dementia
Item
cognitive impairment or dementia.
boolean
C1839000 (UMLS CUI [1])
C0497327 (UMLS CUI [2])
alcohol abuse
Item
current alcohol abuse or dependence
boolean
C0085762 (UMLS CUI [1])

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