ID

37670

Description

Amyloid-related Imaging Abnormalities (Microbleeds) in Atypical AD; ODM derived from: https://clinicaltrials.gov/show/NCT01723553

Lien

https://clinicaltrials.gov/show/NCT01723553

Mots-clés

Versions (1)
  1. 15/08/2019 15/08/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

15 août 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

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Eligibility Atypical Alzheimers Disease NCT01723553

Anglais

Eligibility Atypical Alzheimers Disease NCT01723553

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
over the age of 21
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
will have an informant/study partner who will be able to provide independent evaluation of functioning
Description

Informant Evaluation Functioning

Type de données

boolean

Alias
UMLS CUI [1,1]
C1550484
UMLS CUI [1,2]
C1261322
UMLS CUI [1,3]
C0205245
must fulfill clinical diagnostic criteria for atypical ad, and hence should either have a chief complaint of difficulty with language and fulfill criteria for logopenic variant of primary progressive aphasia, or present with visuospatial/perceptual deficits and fulfill criteria for posterior cortical atrophy
Description

Alzheimer's Disease Atypical | Difficulty using language | Logopenic progressive aphasia | Visuospatial deficit | Perceptual disturbance | Posterior cortical atrophy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0002395
UMLS CUI [1,2]
C0205182
UMLS CUI [2]
C0564213
UMLS CUI [3]
C4274665
UMLS CUI [4]
C2921138
UMLS CUI [5]
C0233746
UMLS CUI [6]
C4275079
speaks english as their primary language (including bilingual patients whose primary language is english)
Description

Primary Language Spoken English | Bilingual person Language primary English

Type de données

boolean

Alias
UMLS CUI [1,1]
C4331028
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0682128
UMLS CUI [2,2]
C1717991
UMLS CUI [2,3]
C0376245
agrees to and is eligible to undergo mri and pet scanning
Description

MRI | PET scan

Type de données

boolean

Alias
UMLS CUI [1]
C0024485
UMLS CUI [2]
C0032743
if woman of child bearing age, must agree to pregnancy test no more than 48 hours before the pet scans
Description

Childbearing Potential Pregnancy Test

Type de données

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0032976
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects with concurrent illnesses that could account for the presenting syndrome, such as traumatic brain injury, strokes or developmental syndromes
Description

Comorbidity | Traumatic Brain Injury | Cerebrovascular accident | Developmental Disabilities

Type de données

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0876926
UMLS CUI [3]
C0038454
UMLS CUI [4]
C0008073
subjects meeting criteria for another neurodegenerative disease, particularly typical alzheimer's dementia
Description

Neurodegenerative Disorder | Dementia of the Alzheimer's type

Type de données

boolean

Alias
UMLS CUI [1]
C0524851
UMLS CUI [2]
C0854732
women that are pregnant or post-partum and breast-feeding
Description

Pregnancy | Postpartum Period | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0086839
UMLS CUI [3]
C0006147
subjects will also be excluded if mri is contraindicated (metal in head, cardiac pace maker, e.t.c.), if there is severe claustrophobia, and if there are conditions that may confound brain imaging studies (e.g. structural abnormalities, including subdural hematoma or intracranial neoplasm)
Description

Medical contraindication MRI | Metal foreign body in head | Artificial cardiac pacemaker | Claustrophobia Severe | Condition Interferes with Imaging of brain | MISCELLANEOUS STRUCTURAL ABNORMALITIES | Hematoma, Subdural | Neoplasms, Intracranial

Type de données

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2]
C0561024
UMLS CUI [3]
C0030163
UMLS CUI [4,1]
C0008909
UMLS CUI [4,2]
C0205082
UMLS CUI [5,1]
C0348080
UMLS CUI [5,2]
C0521102
UMLS CUI [5,3]
C0203860
UMLS CUI [6]
C0333310
UMLS CUI [7]
C0018946
UMLS CUI [8]
C1527390
subjects will also be excluded if they do not have an informant, do not consent to research or do not complete all components of the study (neurological exam, neuropsychometric tests, mri, pib pet)
Description

informant Lacking | Consent Absent Research | Completion Absent Component Clinical Trial | Neurologic Examination | Other Coding | MRI | PET with concurrent CT using C-PiB

Type de données

boolean

Alias
UMLS CUI [1,1]
C1550484
UMLS CUI [1,2]
C0332268
UMLS CUI [2,1]
C1511481
UMLS CUI [2,2]
C0332197
UMLS CUI [2,3]
C0035168
UMLS CUI [3,1]
C0205197
UMLS CUI [3,2]
C0332197
UMLS CUI [3,3]
C1705248
UMLS CUI [3,4]
C0008976
UMLS CUI [4]
C0027853
UMLS CUI [5]
C3846158
UMLS CUI [6]
C0024485
UMLS CUI [7]
C4271886
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Similar models

Eligibility Atypical Alzheimers Disease NCT01723553

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
over the age of 21
boolean
C0001779 (UMLS CUI [1])
Informant Evaluation Functioning
Item
will have an informant/study partner who will be able to provide independent evaluation of functioning
boolean
C1550484 (UMLS CUI [1,1])
C1261322 (UMLS CUI [1,2])
C0205245 (UMLS CUI [1,3])
Alzheimer's Disease Atypical | Difficulty using language | Logopenic progressive aphasia | Visuospatial deficit | Perceptual disturbance | Posterior cortical atrophy
Item
must fulfill clinical diagnostic criteria for atypical ad, and hence should either have a chief complaint of difficulty with language and fulfill criteria for logopenic variant of primary progressive aphasia, or present with visuospatial/perceptual deficits and fulfill criteria for posterior cortical atrophy
boolean
C0002395 (UMLS CUI [1,1])
C0205182 (UMLS CUI [1,2])
C0564213 (UMLS CUI [2])
C4274665 (UMLS CUI [3])
C2921138 (UMLS CUI [4])
C0233746 (UMLS CUI [5])
C4275079 (UMLS CUI [6])
Primary Language Spoken English | Bilingual person Language primary English
Item
speaks english as their primary language (including bilingual patients whose primary language is english)
boolean
C4331028 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0682128 (UMLS CUI [2,1])
C1717991 (UMLS CUI [2,2])
C0376245 (UMLS CUI [2,3])
MRI | PET scan
Item
agrees to and is eligible to undergo mri and pet scanning
boolean
C0024485 (UMLS CUI [1])
C0032743 (UMLS CUI [2])
Childbearing Potential Pregnancy Test
Item
if woman of child bearing age, must agree to pregnancy test no more than 48 hours before the pet scans
boolean
C3831118 (UMLS CUI [1,1])
C0032976 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Comorbidity | Traumatic Brain Injury | Cerebrovascular accident | Developmental Disabilities
Item
subjects with concurrent illnesses that could account for the presenting syndrome, such as traumatic brain injury, strokes or developmental syndromes
boolean
C0009488 (UMLS CUI [1])
C0876926 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0008073 (UMLS CUI [4])
Neurodegenerative Disorder | Dementia of the Alzheimer's type
Item
subjects meeting criteria for another neurodegenerative disease, particularly typical alzheimer's dementia
boolean
C0524851 (UMLS CUI [1])
C0854732 (UMLS CUI [2])
Pregnancy | Postpartum Period | Breast Feeding
Item
women that are pregnant or post-partum and breast-feeding
boolean
C0032961 (UMLS CUI [1])
C0086839 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Medical contraindication MRI | Metal foreign body in head | Artificial cardiac pacemaker | Claustrophobia Severe | Condition Interferes with Imaging of brain | MISCELLANEOUS STRUCTURAL ABNORMALITIES | Hematoma, Subdural | Neoplasms, Intracranial
Item
subjects will also be excluded if mri is contraindicated (metal in head, cardiac pace maker, e.t.c.), if there is severe claustrophobia, and if there are conditions that may confound brain imaging studies (e.g. structural abnormalities, including subdural hematoma or intracranial neoplasm)
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0561024 (UMLS CUI [2])
C0030163 (UMLS CUI [3])
C0008909 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0348080 (UMLS CUI [5,1])
C0521102 (UMLS CUI [5,2])
C0203860 (UMLS CUI [5,3])
C0333310 (UMLS CUI [6])
C0018946 (UMLS CUI [7])
C1527390 (UMLS CUI [8])
informant Lacking | Consent Absent Research | Completion Absent Component Clinical Trial | Neurologic Examination | Other Coding | MRI | PET with concurrent CT using C-PiB
Item
subjects will also be excluded if they do not have an informant, do not consent to research or do not complete all components of the study (neurological exam, neuropsychometric tests, mri, pib pet)
boolean
C1550484 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C1511481 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0035168 (UMLS CUI [2,3])
C0205197 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C1705248 (UMLS CUI [3,3])
C0008976 (UMLS CUI [3,4])
C0027853 (UMLS CUI [4])
C3846158 (UMLS CUI [5])
C0024485 (UMLS CUI [6])
C4271886 (UMLS CUI [7])
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