ID

41590

Beschrijving

The TRUST Study - Depression Substudy; ODM derived from: https://clinicaltrials.gov/show/NCT01853579

Link

https://clinicaltrials.gov/show/NCT01853579

Trefwoorden

Versies (1)
  1. 18-11-20 18-11-20 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

18 november 2020

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Subclinical Hypothyroidism NCT01853579

Engels

Eligibility Subclinical Hypothyroidism NCT01853579

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
community-dwelling patients aged >= 65 years with subclinical hypothyroidism
Beschrijving

community-dwelling patients aged >= 65 years with subclinical hypothyroidism

Datatype

boolean

Alias
UMLS CUI [1]
C4045975
UMLS CUI [2]
C0001779
UMLS CUI [3,1]
C0020676
UMLS CUI [3,2]
C0205211
written informed consent
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
subjects currently on levothyroxine or antithyroid drugs, amiodarone or lithium
Beschrijving

currently on levothyroxine or antithyroid drugs, amiodarone or lithium

Datatype

boolean

Alias
UMLS CUI [1,1]
C2827774
UMLS CUI [1,2]
C0040165
UMLS CUI [2,1]
C2827774
UMLS CUI [2,2]
C0040125
UMLS CUI [3,1]
C2827774
UMLS CUI [3,2]
C0002598
UMLS CUI [4,1]
C2827774
UMLS CUI [4,2]
C0023870
recent thyroid surgery or radio-iodine (within 12 months)
Beschrijving

recent thyroid surgery or radio-iodine

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332185
UMLS CUI [1,2]
C0193769
UMLS CUI [2,1]
C0332185
UMLS CUI [2,2]
C2169308
grade iv nyha heart failure
Beschrijving

grade iv nyha heart failure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
prior clinical diagnosis of dementia
Beschrijving

prior clinical diagnosis of dementia

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332132
UMLS CUI [1,2]
C0497327
recent hospitalisation for major illness or elective surgery (within 4 weeks)
Beschrijving

recent hospitalisation for major illness or elective surgery

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332185
UMLS CUI [1,2]
C0019993
UMLS CUI [1,3]
C0221423
UMLS CUI [1,4]
C0205164
UMLS CUI [2,1]
C0332185
UMLS CUI [2,2]
C0019993
UMLS CUI [2,3]
C0206058
terminal illness
Beschrijving

terminal illness

Datatype

boolean

Alias
UMLS CUI [1]
C0679247
patients with hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption
Beschrijving

rare hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption

Datatype

boolean

Alias
UMLS CUI [1,1]
C0016952
UMLS CUI [1,2]
C0439660
UMLS CUI [2,1]
C0337904
UMLS CUI [2,2]
C0302813
UMLS CUI [3]
C0268186
subjects who are participating in ongoing rcts of therapeutic interventions (including ctimps)
Beschrijving

participation in ongoing rcts

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0549178
UMLS CUI [1,3]
C0206035
plan to move out of the region in which the trial is being conducted within the next 2 years (proposed minimum follow-up period)
Beschrijving

plan to move out of the region in which the trial is being conducted within the next 2 years

Datatype

boolean

Alias
UMLS CUI [1,1]
C2699029
UMLS CUI [1,2]
C1301732
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Similar models

Eligibility Subclinical Hypothyroidism NCT01853579

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
community-dwelling patients aged >= 65 years with subclinical hypothyroidism
Item
community-dwelling patients aged >= 65 years with subclinical hypothyroidism
boolean
C4045975 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0020676 (UMLS CUI [3,1])
C0205211 (UMLS CUI [3,2])
informed consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
currently on levothyroxine or antithyroid drugs, amiodarone or lithium
Item
subjects currently on levothyroxine or antithyroid drugs, amiodarone or lithium
boolean
C2827774 (UMLS CUI [1,1])
C0040165 (UMLS CUI [1,2])
C2827774 (UMLS CUI [2,1])
C0040125 (UMLS CUI [2,2])
C2827774 (UMLS CUI [3,1])
C0002598 (UMLS CUI [3,2])
C2827774 (UMLS CUI [4,1])
C0023870 (UMLS CUI [4,2])
recent thyroid surgery or radio-iodine
Item
recent thyroid surgery or radio-iodine (within 12 months)
boolean
C0332185 (UMLS CUI [1,1])
C0193769 (UMLS CUI [1,2])
C0332185 (UMLS CUI [2,1])
C2169308 (UMLS CUI [2,2])
grade iv nyha heart failure
Item
grade iv nyha heart failure
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
prior clinical diagnosis of dementia
Item
prior clinical diagnosis of dementia
boolean
C0332132 (UMLS CUI [1,1])
C0497327 (UMLS CUI [1,2])
recent hospitalisation for major illness or elective surgery
Item
recent hospitalisation for major illness or elective surgery (within 4 weeks)
boolean
C0332185 (UMLS CUI [1,1])
C0019993 (UMLS CUI [1,2])
C0221423 (UMLS CUI [1,3])
C0205164 (UMLS CUI [1,4])
C0332185 (UMLS CUI [2,1])
C0019993 (UMLS CUI [2,2])
C0206058 (UMLS CUI [2,3])
terminal illness
Item
terminal illness
boolean
C0679247 (UMLS CUI [1])
rare hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption
Item
patients with hereditary problems of galactose intolerance, the lapp lactase deficiency or glucose-galactose malabsorption
boolean
C0016952 (UMLS CUI [1,1])
C0439660 (UMLS CUI [1,2])
C0337904 (UMLS CUI [2,1])
C0302813 (UMLS CUI [2,2])
C0268186 (UMLS CUI [3])
participation in ongoing rcts
Item
subjects who are participating in ongoing rcts of therapeutic interventions (including ctimps)
boolean
C2348568 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
C0206035 (UMLS CUI [1,3])
plan to move out of the region in which the trial is being conducted within the next 2 years
Item
plan to move out of the region in which the trial is being conducted within the next 2 years (proposed minimum follow-up period)
boolean
C2699029 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
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