Informationen:
Fehler:
ID
43873
Beschreibung
Lilly's Emotional and Physical Symptoms of Depression Study; ODM derived from: https://clinicaltrials.gov/show/NCT00479414
Link
https://clinicaltrials.gov/show/NCT00479414
Stichworte
Versionen (3)
- 18.10.16 18.10.16 -
- 19.10.16 19.10.16 -
- 20.09.21 20.09.21 -
Hochgeladen am
20. September 2021
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Major Depressive Disorder NCT00479414
Eligibility Major Depressive Disorder NCT00479414
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Major Depressive Disorder NCT00479414
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Major Depressive Disorder
Item
meet criteria for major depressive disorder according to the dsm-iv diagnostic criteria
boolean
C1269683 (UMLS CUI [1])
Outpatients | Age
Item
outpatients at least 18 years of age
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Informed Consent
Item
sign the informed consent
boolean
C0021430 (UMLS CUI [1])
Gender Urine pregnancy test negative | Childbearing Potential Contraceptive methods
Item
all females must test negative for a urine pregnancy test at visit 1. females of child bearing potential must agree to utilize medically acceptable and reliable means of birth control
boolean
C0079399 (UMLS CUI [1,1])
C0430057 (UMLS CUI [1,2])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0430057 (UMLS CUI [1,2])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Able to communicate Investigator | Depression self rating scale Completion Ability
Item
have a level of understanding sufficient to communicate with the investigator and are able to complete all patient self-rated scales in the study
boolean
C2364293 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
C0451108 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0085732 (UMLS CUI [2,3])
C0035173 (UMLS CUI [1,2])
C0451108 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
C0085732 (UMLS CUI [2,3])
Research Personnel Affiliated Clinical Trial Family | Research Personnel Affiliated Immediate family
Item
are investigator site personnel directly affiliated with the study or immediate family.
boolean
C0035173 (UMLS CUI [1,1])
C1510826 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0015576 (UMLS CUI [1,4])
C0035173 (UMLS CUI [2,1])
C1510826 (UMLS CUI [2,2])
C2371717 (UMLS CUI [2,3])
C1510826 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0015576 (UMLS CUI [1,4])
C0035173 (UMLS CUI [2,1])
C1510826 (UMLS CUI [2,2])
C2371717 (UMLS CUI [2,3])
Employee Eli Lilly & Co Ltd
Item
are employed by eli lilly and company
boolean
C0599987 (UMLS CUI [1,1])
C0470942 (UMLS CUI [1,2])
C0470942 (UMLS CUI [1,2])
Study Subject Participation Status | Therapeutic procedure Drug Approval Lacking
Item
have received treatment within the last 30 days or are currently enrolled in a study with a drug that has not received regulatory approval for any indication at time of study entry
boolean
C2348568 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0162696 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
C0087111 (UMLS CUI [2,1])
C0162696 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
Substance Dependence | Nicotine Dependence | Caffeine dependence
Item
current substance dependence, excluding nicotine and caffeine
boolean
C0038580 (UMLS CUI [1])
C0028043 (UMLS CUI [2])
C1386553 (UMLS CUI [3])
C0028043 (UMLS CUI [2])
C1386553 (UMLS CUI [3])
Monoamine Oxidase Inhibitors
Item
treatment with a monoamine oxidase inhibitor within 14 days prior to visit 1 or potential need to use an maoi within 5 days after discontinuation of study drug
boolean
C0026457 (UMLS CUI [1])
Injury of liver | Liver Cirrhosis Severe | Child-Pugh Classification
Item
acute live injury or severe (child-pugh class c) cirrhosis
boolean
C0160390 (UMLS CUI [1])
C0023890 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C4050412 (UMLS CUI [3])
C0023890 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C4050412 (UMLS CUI [3])