ID

23240

Beschrijving

Does Dual Therapy Hasten Antidepressant Response?; ODM derived from: https://clinicaltrials.gov/show/NCT00519428

Link

https://clinicaltrials.gov/show/NCT00519428

Trefwoorden

  1. 30-06-17 30-06-17 -
Geüploaded op

30 juni 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Major Depressive Disorder NCT00519428

Eligibility Major Depressive Disorder NCT00519428

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. men and women ages 18-65
Beschrijving

ID.1

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
2. major depressive disorder as primary diagnosis
Beschrijving

ID.2

Datatype

boolean

Alias
UMLS CUI [1]
C1269683
3. physically healthy
Beschrijving

ID.3

Datatype

boolean

Alias
UMLS CUI [1]
C0018684
4. signs informed consent
Beschrijving

ID.4

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
5. montgomery asberg depression rating scale (madrs) >= 22
Beschrijving

ID.5

Datatype

boolean

Alias
UMLS CUI [1]
C4054475
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. bipolar disorder (ie, bipolar i, bipolar ii, bipolar nos)
Beschrijving

ID.6

Datatype

boolean

Alias
UMLS CUI [1]
C0005586
2. life-time history of psychosis
Beschrijving

ID.7

Datatype

boolean

Alias
UMLS CUI [1]
C0033975
3. current (ie, last 6 months) drug or alcohol abuse or dependence (except nicotine)
Beschrijving

ID.8

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085762
UMLS CUI [1,2]
C0013146
4. currently taking effective antidepressant medication
Beschrijving

ID.9

Datatype

boolean

Alias
UMLS CUI [1]
C0003289
5. prior adequate treatment in current depressive episode with a ssri, bup or bup + ssri ("adequate" is defined as >= 4 weeks taking >= 2/3 pdr maximal dose)
Beschrijving

ID.10

Datatype

boolean

Alias
UMLS CUI [1]
C0003289
6. most recent antidepressant was within 5 weeks for fluoxetine and 1 week for all others
Beschrijving

ID.11

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003289
UMLS CUI [1,2]
C0016365
7. currently taking a medication contraindicated with either study medication
Beschrijving

ID.12

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1444657
8. life time history of anorexia or bulimia
Beschrijving

ID.13

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003123
UMLS CUI [1,2]
C0006370
9. life time history of seizure or known increased seizure risk (e.g., history of significant brain trauma, taking pro-convulsant medication, known anatomical brain lesion)
Beschrijving

ID.14

Datatype

boolean

Alias
UMLS CUI [1]
C0036572
10. currently taking psychoactive medication deemed to be necessary (including but not limited anticonvulsants, antidepressants, antipsychotics, steroids, and b-blockers); occasional use of hypnotics (ie, less than three times per week) will be allowed
Beschrijving

ID.15

Datatype

boolean

Alias
UMLS CUI [1]
C2065419
11. unstable medical condition (ie, condition not adequately stabilized for >= 3 months)
Beschrijving

ID.16

Datatype

boolean

Alias
UMLS CUI [1]
C0012634
12. prior intolerance to esc or bup
Beschrijving

ID.17

Datatype

boolean

Alias
UMLS CUI [1]
C0020517
13. inadequate understanding of english (for us site; canadian site permits french fluency)
Beschrijving

ID.18

Datatype

boolean

Alias
UMLS CUI [1]
C1145677
14. currently pregnant or breast-feeding; fecund women not using adequate contraceptive methods
Beschrijving

ID.19

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
UMLS CUI [1,3]
C0009862

Similar models

Eligibility Major Depressive Disorder NCT00519428

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
1. men and women ages 18-65
boolean
C0001779 (UMLS CUI [1])
ID.2
Item
2. major depressive disorder as primary diagnosis
boolean
C1269683 (UMLS CUI [1])
ID.3
Item
3. physically healthy
boolean
C0018684 (UMLS CUI [1])
ID.4
Item
4. signs informed consent
boolean
C0021430 (UMLS CUI [1])
ID.5
Item
5. montgomery asberg depression rating scale (madrs) >= 22
boolean
C4054475 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.6
Item
1. bipolar disorder (ie, bipolar i, bipolar ii, bipolar nos)
boolean
C0005586 (UMLS CUI [1])
ID.7
Item
2. life-time history of psychosis
boolean
C0033975 (UMLS CUI [1])
ID.8
Item
3. current (ie, last 6 months) drug or alcohol abuse or dependence (except nicotine)
boolean
C0085762 (UMLS CUI [1,1])
C0013146 (UMLS CUI [1,2])
ID.9
Item
4. currently taking effective antidepressant medication
boolean
C0003289 (UMLS CUI [1])
ID.10
Item
5. prior adequate treatment in current depressive episode with a ssri, bup or bup + ssri ("adequate" is defined as >= 4 weeks taking >= 2/3 pdr maximal dose)
boolean
C0003289 (UMLS CUI [1])
ID.11
Item
6. most recent antidepressant was within 5 weeks for fluoxetine and 1 week for all others
boolean
C0003289 (UMLS CUI [1,1])
C0016365 (UMLS CUI [1,2])
ID.12
Item
7. currently taking a medication contraindicated with either study medication
boolean
C0013227 (UMLS CUI [1,1])
C1444657 (UMLS CUI [1,2])
ID.13
Item
8. life time history of anorexia or bulimia
boolean
C0003123 (UMLS CUI [1,1])
C0006370 (UMLS CUI [1,2])
ID.14
Item
9. life time history of seizure or known increased seizure risk (e.g., history of significant brain trauma, taking pro-convulsant medication, known anatomical brain lesion)
boolean
C0036572 (UMLS CUI [1])
ID.15
Item
10. currently taking psychoactive medication deemed to be necessary (including but not limited anticonvulsants, antidepressants, antipsychotics, steroids, and b-blockers); occasional use of hypnotics (ie, less than three times per week) will be allowed
boolean
C2065419 (UMLS CUI [1])
ID.16
Item
11. unstable medical condition (ie, condition not adequately stabilized for >= 3 months)
boolean
C0012634 (UMLS CUI [1])
ID.17
Item
12. prior intolerance to esc or bup
boolean
C0020517 (UMLS CUI [1])
ID.18
Item
13. inadequate understanding of english (for us site; canadian site permits french fluency)
boolean
C1145677 (UMLS CUI [1])
ID.19
Item
14. currently pregnant or breast-feeding; fecund women not using adequate contraceptive methods
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
C0009862 (UMLS CUI [1,3])

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