ID

12590

Description

Subanesthetic IV Bolus Ketamine in the Treatment of Acute Depression; ODM derived from: https://clinicaltrials.gov/show/NCT02378415

Link

https://clinicaltrials.gov/show/NCT02378415

Keywords

Versions (1)
  1. 03/12/2015 03/12/2015 -
Uploaded on

3 de dezembro de 2015

DOI

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License

Creative Commons BY 4.0
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Eligibility Acute Depression NCT02378415

English

Eligibility Acute Depression NCT02378415

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
bss greater than 4
Description

bss greater than 4

Data type

boolean

Alias
UMLS CUI [1]
N
bhs greater than 8
Description

bhs greater than 8

Data type

boolean

Alias
UMLS CUI [1]
N
bdi greater than 19
Description

bdi greater than 19

Data type

boolean

Alias
UMLS CUI [1]
C0451022
ability to give informed consent.
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
active duty military status.
Description

active duty military status

Data type

boolean

Alias
UMLS CUI [1]
C2129059
verified negative qualitative pregnancy test.
Description

pregnancy test

Data type

boolean

Alias
UMLS CUI [1]
C0032976
all participants must be accepted for psychiatric admission to the hospital prior to consideration for enrollment in this study.
Description

psychiatric admission to the hospital

Data type

boolean

Alias
UMLS CUI [1]
C0237457
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
psychosis or bipolar disorder.
Description

psychosis or bipolar disorder

Data type

boolean

Alias
UMLS CUI [1]
C0033975
UMLS CUI [2]
C0005586
pregnancy
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0549206
involuntary status on presentation to the ed.
Description

involuntary status

Data type

boolean

Alias
UMLS CUI [1]
C0745037
uds positive for illicit drugs of abuse.
Description

uds positive for illicit drugs of abuse

Data type

boolean

Alias
UMLS CUI [1]
C0038586
blood alcohol level greater than zero
Description

blood alcohol level greater than zero

Data type

boolean

Alias
UMLS CUI [1]
C0038586
previous enrollees in this treatment protocol will be excluded from repeat participation.
Description

previous enrollees in this treatment protocol will be excluded from repeat participation

Data type

boolean

Alias
UMLS CUI [1]
C2348568
any patient brought for command directed psychiatric evaluation.
Description

command directed psychiatric evaluation

Data type

boolean

Alias
UMLS CUI [1]
C0846574
specific contraindications to the use of ketamine are as follows and under such circumstances or conditions, personnel with the following should be excluded from participation in this study:
Description

specific contraindications to the use of ketamine

Data type

boolean

Alias
UMLS CUI [1]
C0522473
UMLS CUI [2]
C0022614
patients with elevated intracranial pressure, uncontrolled hypertension, coronary artery disease, aneurysms, thyrotoxicosis, chf, a recent history of head or eye injury, or angina.
Description

patients with elevated intracranial pressure, uncontrolled hypertension, coronary artery disease, aneurysms, thyrotoxicosis, chf, a recent history of head or eye injury, or angina

Data type

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C1301624
all personnel in whom a significant elevation of blood pressure would constitute a serious hazard to their overall health and well-being.
Description

all personnel in whom a significant elevation of blood pressure would constitute a serious hazard to their overall health and well-being.

Data type

boolean

Alias
UMLS CUI [1]
C0525058
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
patients currently utilizing the following medications: conivaptan, disatinib, peginterferon alfa-2b, quazepam, tocilizumab
Description

patients currently utilizing the following medications: conivaptan, disatinib, peginterferon alfa-2b, quazepam, tocilizumab

Data type

boolean

Alias
UMLS CUI [1]
C0525058
UMLS CUI [2]
C0439801
UMLS CUI [3]
C0009488
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Similar models

Eligibility Acute Depression NCT02378415

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
bss greater than 4
Item
bss greater than 4
boolean
N (UMLS CUI [1])
bhs greater than 8
Item
bhs greater than 8
boolean
N (UMLS CUI [1])
bdi greater than 19
Item
bdi greater than 19
boolean
C0451022 (UMLS CUI [1])
informed consent
Item
ability to give informed consent.
boolean
C0021430 (UMLS CUI [1])
active duty military status
Item
active duty military status.
boolean
C2129059 (UMLS CUI [1])
pregnancy test
Item
verified negative qualitative pregnancy test.
boolean
C0032976 (UMLS CUI [1])
psychiatric admission to the hospital
Item
all participants must be accepted for psychiatric admission to the hospital prior to consideration for enrollment in this study.
boolean
C0237457 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
psychosis or bipolar disorder
Item
psychosis or bipolar disorder.
boolean
C0033975 (UMLS CUI [1])
C0005586 (UMLS CUI [2])
pregnancy
Item
pregnancy
boolean
C0549206 (UMLS CUI [1])
involuntary status
Item
involuntary status on presentation to the ed.
boolean
C0745037 (UMLS CUI [1])
uds positive for illicit drugs of abuse
Item
uds positive for illicit drugs of abuse.
boolean
C0038586 (UMLS CUI [1])
blood alcohol level greater than zero
Item
blood alcohol level greater than zero
boolean
C0038586 (UMLS CUI [1])
previous enrollees in this treatment protocol will be excluded from repeat participation
Item
previous enrollees in this treatment protocol will be excluded from repeat participation.
boolean
C2348568 (UMLS CUI [1])
command directed psychiatric evaluation
Item
any patient brought for command directed psychiatric evaluation.
boolean
C0846574 (UMLS CUI [1])
specific contraindications to the use of ketamine
Item
specific contraindications to the use of ketamine are as follows and under such circumstances or conditions, personnel with the following should be excluded from participation in this study:
boolean
C0522473 (UMLS CUI [1])
C0022614 (UMLS CUI [2])
patients with elevated intracranial pressure, uncontrolled hypertension, coronary artery disease, aneurysms, thyrotoxicosis, chf, a recent history of head or eye injury, or angina
Item
patients with elevated intracranial pressure, uncontrolled hypertension, coronary artery disease, aneurysms, thyrotoxicosis, chf, a recent history of head or eye injury, or angina.
boolean
C0009488 (UMLS CUI [1])
C1301624 (UMLS CUI [2])
all personnel in whom a significant elevation of blood pressure would constitute a serious hazard to their overall health and well-being.
Item
all personnel in whom a significant elevation of blood pressure would constitute a serious hazard to their overall health and well-being.
boolean
C0525058 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
patients currently utilizing the following medications: conivaptan, disatinib, peginterferon alfa-2b, quazepam, tocilizumab
Item
patients currently utilizing the following medications: conivaptan, disatinib, peginterferon alfa-2b, quazepam, tocilizumab
boolean
C0525058 (UMLS CUI [1])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])
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