ID

15299

Beschrijving

Pharmacotherapy in Depression With Panic Spectrum; ODM derived from: https://clinicaltrials.gov/show/NCT00177996

Link

https://clinicaltrials.gov/show/NCT00177996

Trefwoorden

  1. 2016-05-25 2016-05-25 -
  2. 2016-05-25 2016-05-25 -
Geüploaded op

25 maj 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Major Depression NCT00177996

Eligibility Major Depression NCT00177996

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female ages 18-60;
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
current diagnosis of major depression, and a rating of ³15 on the hrs-d-25; --presence of significant, co-existing panic-agoraphobic spectrum symptoms,
Beschrijving

major depression

Datatype

boolean

Alias
UMLS CUI [1]
C1269683
absence of ongoing therapy with psychotropic medications (except for intermittent use of nonbenzodiazepine hypnotics) or willingness to be withdrawn from an ineffective ongoing antidepressant medications
Beschrijving

therapy with psychotropic medications

Datatype

boolean

Alias
UMLS CUI [1]
C0033978
physically healthy,
Beschrijving

physically healthy

Datatype

boolean

Alias
UMLS CUI [1]
C0018759
female participants of childbearing potential must be practicing a medically acceptable form of double-barrier birth control or using oral contraceptives such as birth control pills, implants, or injections;
Beschrijving

contraceptive use

Datatype

boolean

Alias
UMLS CUI [1]
C1999124
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
females who are pregnant or breast-feeding;
Beschrijving

pregnant or breast-feeding

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
history of suicide attempt in the 6 months prior to entry, active suicidal ideation, or significant suicide risk;
Beschrijving

history of suicide attempt

Datatype

boolean

Alias
UMLS CUI [1]
C0038663
UMLS CUI [2]
C0438696
history of hypersensitivity to or current use of sertraline;
Beschrijving

history of hypersensitivity

Datatype

boolean

Alias
UMLS CUI [1]
C0020517
UMLS CUI [2]
C0074393
unstable or untreated medical conditions,
Beschrijving

untreated medical conditions

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
participants who do not wish to discontinue current, ineffective antidepressant treatment;
Beschrijving

discontinue antidepressant treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003289
UMLS CUI [1,2]
C1518544
participants who have recently begun psychotherapy (less than 3 months prior to study entry);
Beschrijving

psychotherapy

Datatype

boolean

Alias
UMLS CUI [1]
C0033968
diagnosis of current panic disorder, psychosis, substance or alcohol abuse, anorexia, bulimia, dissociative, bipolar disorder, or any other psychiatric or medical illness that would interfere with the best treatment strategy for the potential participant.
Beschrijving

exclusion diagnoses

Datatype

boolean

Alias
UMLS CUI [1]
C0030319
UMLS CUI [2]
C0033975
UMLS CUI [3]
C0038586
UMLS CUI [4]
C0003123
UMLS CUI [5]
C0006370
UMLS CUI [6]
C0005586

Similar models

Eligibility Major Depression NCT00177996

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
male or female ages 18-60;
boolean
C0001779 (UMLS CUI [1])
major depression
Item
current diagnosis of major depression, and a rating of ³15 on the hrs-d-25; --presence of significant, co-existing panic-agoraphobic spectrum symptoms,
boolean
C1269683 (UMLS CUI [1])
therapy with psychotropic medications
Item
absence of ongoing therapy with psychotropic medications (except for intermittent use of nonbenzodiazepine hypnotics) or willingness to be withdrawn from an ineffective ongoing antidepressant medications
boolean
C0033978 (UMLS CUI [1])
physically healthy
Item
physically healthy,
boolean
C0018759 (UMLS CUI [1])
contraceptive use
Item
female participants of childbearing potential must be practicing a medically acceptable form of double-barrier birth control or using oral contraceptives such as birth control pills, implants, or injections;
boolean
C1999124 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnant or breast-feeding
Item
females who are pregnant or breast-feeding;
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
history of suicide attempt
Item
history of suicide attempt in the 6 months prior to entry, active suicidal ideation, or significant suicide risk;
boolean
C0038663 (UMLS CUI [1])
C0438696 (UMLS CUI [2])
history of hypersensitivity
Item
history of hypersensitivity to or current use of sertraline;
boolean
C0020517 (UMLS CUI [1])
C0074393 (UMLS CUI [2])
untreated medical conditions
Item
unstable or untreated medical conditions,
boolean
C0009488 (UMLS CUI [1])
discontinue antidepressant treatment
Item
participants who do not wish to discontinue current, ineffective antidepressant treatment;
boolean
C0003289 (UMLS CUI [1,1])
C1518544 (UMLS CUI [1,2])
psychotherapy
Item
participants who have recently begun psychotherapy (less than 3 months prior to study entry);
boolean
C0033968 (UMLS CUI [1])
exclusion diagnoses
Item
diagnosis of current panic disorder, psychosis, substance or alcohol abuse, anorexia, bulimia, dissociative, bipolar disorder, or any other psychiatric or medical illness that would interfere with the best treatment strategy for the potential participant.
boolean
C0030319 (UMLS CUI [1])
C0033975 (UMLS CUI [2])
C0038586 (UMLS CUI [3])
C0003123 (UMLS CUI [4])
C0006370 (UMLS CUI [5])
C0005586 (UMLS CUI [6])

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