Informazione:
Errore:
ID
16319
Descrizione
A Randomised Trial of Sertraline, Cognitive Behaviour Therapy & Combined Therapy for Postnatal Depression; ODM derived from: https://clinicaltrials.gov/show/NCT02122393
collegamento
https://clinicaltrials.gov/show/NCT02122393
Keywords
versioni (1)
- 11/07/16 11/07/16 -
Caricato su
11 luglio 2016
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
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Eligibility Depression NCT02122393
Eligibility Depression NCT02122393
- StudyEvent: Eligibility
Similar models
Eligibility Depression NCT02122393
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
women, childs age
Item
women with an infant > 2 months and < 8 months of age
boolean
C0026591 (UMLS CUI [1])
infant born after a full-term pregnancy
Item
infant born after a full-term pregnancy
boolean
C2114495 (UMLS CUI [1])
congenital abnormalities
Item
infant born with no congenital abnormalities
boolean
C0000768 (UMLS CUI [1])
postnatal depression
Item
diagnosis of depression with postnatal onset according to the diagnostic and statistical manual of mental disorders 4th edition (dsm-iv).
boolean
C0221074 (UMLS CUI [1])
positive serum pregnancy test
Item
positive serum pregnancy test;
boolean
C0430063 (UMLS CUI [1])
concurrent psychiatric disorder
Item
concurrent psychiatric disorder (excepting co-morbid anxiety);
boolean
C0004936 (UMLS CUI [1])
recent history of antidepressant usage
Item
recent history of antidepressant usage (within the last month);
boolean
C0262926 (UMLS CUI [1,1])
C0003289 (UMLS CUI [1,2])
C0003289 (UMLS CUI [1,2])
major or drug allergy
Item
history of major allergy or drug allergy;
boolean
C0013182 (UMLS CUI [1])
history of substance abuse
Item
history of substance abuse;
boolean
C0038586 (UMLS CUI [1])
response to sertraline or ssri
Item
prior non-response to sertraline, or prior non-response to adequate trials of two selective serotonin reuptake inhibitors (ssris);
boolean
C0871261 (UMLS CUI [1,1])
C0074393 (UMLS CUI [1,2])
C0871261 (UMLS CUI [2,1])
C0360105 (UMLS CUI [2,2])
C0074393 (UMLS CUI [1,2])
C0871261 (UMLS CUI [2,1])
C0360105 (UMLS CUI [2,2])
predisposition to headache, migraine or nausea
Item
predisposition to headache, migraine or nausea;
boolean
C1504388 (UMLS CUI [1,1])
C0018681 (UMLS CUI [1,2])
C1504388 (UMLS CUI [2,1])
C0149931 (UMLS CUI [2,2])
C1504388 (UMLS CUI [3,1])
C0027497 (UMLS CUI [3,2])
C0018681 (UMLS CUI [1,2])
C1504388 (UMLS CUI [2,1])
C0149931 (UMLS CUI [2,2])
C1504388 (UMLS CUI [3,1])
C0027497 (UMLS CUI [3,2])
smoking behaviour
Item
tobacco habit in excess of 10 cigarettes per day;
boolean
C0453996 (UMLS CUI [1])
caffeine consumption
Item
caffeine consumption in excess of 6 cups of coffee/tea or cola-flavoured drinks per day;
boolean
C0948365 (UMLS CUI [1])
dental procedures
Item
ongoing dental work;
boolean
C0011331 (UMLS CUI [1])
severe psychotic depression
Item
extreme levels of depression (psychotic);
boolean
C0270458 (UMLS CUI [1])
suicidal intent
Item
suicidal intent;
boolean
C0582496 (UMLS CUI [1])
study trial participation status
Item
participation in any medical trial within the previous three months;
boolean
C2348568 (UMLS CUI [1])