Informações:
Falhas:
ID
22309
Descrição
Does Sleep Quality Change After Switch From Wellbutrin SR to Wellbutrin XL in Patients With Major Depressive Disorder?; ODM derived from: https://clinicaltrials.gov/show/NCT00616915
Link
https://clinicaltrials.gov/show/NCT00616915
Palavras-chave
Versões (1)
- 29/05/2017 29/05/2017 -
Transferido a
29 de maio de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Mood Disorder NCT00616915
Eligibility Mood Disorder NCT00616915
- StudyEvent: Eligibility
Similar models
Eligibility Mood Disorder NCT00616915
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
informed consent
Item
1. signed patient informed consent;
boolean
C0021430 (UMLS CUI [1])
DSM IV major depressive disorder
Item
2. patients with major depressive disorders (dsm-iv-tr - criteria used);
boolean
C1269683 (UMLS CUI [1,1])
C2199206 (UMLS CUI [1,2])
C2199206 (UMLS CUI [1,2])
outpatients
Item
3. out-patients;
boolean
C0029921 (UMLS CUI [1])
age, gender
Item
4. males or females over 18 years of age;
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
C0079399 (UMLS CUI [2])
wellbutrin sr
Item
5. patients currently using wellbutrin sr.
boolean
C0724393 (UMLS CUI [1,1])
C0746467 (UMLS CUI [1,2])
C0746467 (UMLS CUI [1,2])
bipolar disorder
Item
1. bipolar disorder patients;
boolean
C0005586 (UMLS CUI [1])
actively suicidal
Item
2. actively suicidal patients;
boolean
C0438696 (UMLS CUI [1])
schizophrenia, schizoaffective or other psychotic disorder
Item
3. schizophrenia, schizoaffective or other psychotic disorder;
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
C0033975 (UMLS CUI [3])
C0036337 (UMLS CUI [2])
C0033975 (UMLS CUI [3])
pregnancy
Item
4. pregnant women, as by pregnancy test at the beginning of the study;
boolean
C0032961 (UMLS CUI [1])
women in childbearing age refusing to use contraception, breastfeeding mothers
Item
5. women in childbearing age, refusing to use appropriate contraception, or breastfeeding mothers;
boolean
C1960468 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2])
hypersensitivity to bupropion
Item
6. patients with known hypersensitivity to bupropion;
boolean
C0020517 (UMLS CUI [1,1])
C0085208 (UMLS CUI [1,2])
C0085208 (UMLS CUI [1,2])
severe or unstable comorbidity
Item
7. patients with severe or unstable medical conditions, which in the opinion of the investigator would interfere with their progress or safety;
boolean
C0443343 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
C0205082 (UMLS CUI [2,1])
C0009488 (UMLS CUI [2,2])
C0009488 (UMLS CUI [1,2])
C0205082 (UMLS CUI [2,1])
C0009488 (UMLS CUI [2,2])
ect or tms treatment
Item
8. ect or tms treatments within the last three months;
boolean
C0013806 (UMLS CUI [1])
C0436548 (UMLS CUI [2])
C0436548 (UMLS CUI [2])
non-responder bupropion
Item
9. patients who did not respond to previous treatment with bupropion;
boolean
C0919875 (UMLS CUI [1,1])
C0085208 (UMLS CUI [1,2])
C0085208 (UMLS CUI [1,2])
seizure disorder
Item
10. patients with history of seizure disorder;
boolean
C0014544 (UMLS CUI [1])
eating disorders
Item
11. patients with history of eating disorders (e.g. bulimia, anorexia nervosa);
boolean
C0013473 (UMLS CUI [1])
sleep aiding medication
Item
12. patients using sleep aiding medication (benzodiazepines, barbiturates).
boolean
C2054158 (UMLS CUI [1])