Informationen:
Fehler:
ID
19362
Beschreibung
Comparison of Intramuscular Olanzapine and Intramuscular Haloperidol in Patients With Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00485901
Link
https://clinicaltrials.gov/show/NCT00485901
Stichworte
Versionen (1)
- 21.12.16 21.12.16 -
Hochgeladen am
21. Dezember 2016
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Schizophrenia NCT00485901
Eligibility Schizophrenia NCT00485901
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Schizophrenia NCT00485901
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age
Item
male or female patients, between the ages of 18 and 65
boolean
C0001779 (UMLS CUI [1])
Schizophrenia
Item
patients must have diagnosis of schizophrenia that meets disease diagnostic criteria as defined in dsm-iv
boolean
C0036341 (UMLS CUI [1])
Agitated Clinical | Indication Pharmaceutical Preparations Intramuscular | olanzapine Intramuscular | Comparator Drug Intramuscular | drug safety
Item
patients must be considered, by the investigator, to be clinically agitated and appropriate candidates for treatment with im medication. investigator must believe that it is safe to administer im olanzapine and im comparator to the patients with respect to the safety profile of these drugs (including the anticholinergic properties of olanzapine im or the comparator agent)
boolean
C0085631 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0013227 (UMLS CUI [2,2])
C1556154 (UMLS CUI [2,3])
C0171023 (UMLS CUI [3,1])
C1556154 (UMLS CUI [3,2])
C2347178 (UMLS CUI [4,1])
C1556154 (UMLS CUI [4,2])
C0678800 (UMLS CUI [5])
C0205210 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C0013227 (UMLS CUI [2,2])
C1556154 (UMLS CUI [2,3])
C0171023 (UMLS CUI [3,1])
C1556154 (UMLS CUI [3,2])
C2347178 (UMLS CUI [4,1])
C1556154 (UMLS CUI [4,2])
C0678800 (UMLS CUI [5])
Illness caused by Substance Use Disorders
Item
subjects' illness must not, in the opinion of the investigator, be caused by substance abuse
boolean
C0221423 (UMLS CUI [1,1])
C0015127 (UMLS CUI [1,2])
C0038586 (UMLS CUI [1,3])
C0015127 (UMLS CUI [1,2])
C0038586 (UMLS CUI [1,3])
Hospitalization
Item
patient must be hospitalized during the study
boolean
C0019993 (UMLS CUI [1])
Study Subject Participation Status | Clinical Trial olanzapine Intramuscular
Item
previous participation (treatment with study drug) in a lilly sponsored intra-muscular olanzapine clinical trial
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C0171023 (UMLS CUI [2,2])
C1556154 (UMLS CUI [2,3])
C0008976 (UMLS CUI [2,1])
C0171023 (UMLS CUI [2,2])
C1556154 (UMLS CUI [2,3])
Illness Unstable Serious | Cessation of life Anticipated | Disease Intensive care unit Anticipated
Item
serious, unstable illnesses such that death is anticipated within 1 year or intensive care unit hospitalization for the disease is anticipated within 6 months
boolean
C0221423 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,3])
C0011065 (UMLS CUI [2,1])
C3840775 (UMLS CUI [2,2])
C0012634 (UMLS CUI [3,1])
C0021708 (UMLS CUI [3,2])
C3840775 (UMLS CUI [3,3])
C0443343 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,3])
C0011065 (UMLS CUI [2,1])
C3840775 (UMLS CUI [2,2])
C0012634 (UMLS CUI [3,1])
C0021708 (UMLS CUI [3,2])
C3840775 (UMLS CUI [3,3])
Dementia Type Any
Item
have a known diagnosis of dementia of any type, as defined in the dsm-iv or dsm-iv-tr
boolean
C0497327 (UMLS CUI [1,1])
C0332307 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,2])
C1552551 (UMLS CUI [1,3])
Allergic Reaction Investigational New Drugs
Item
documented history of allergic reaction to study medication(s)
boolean
C1527304 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
Injection of depot antipsychotic agent
Item
treatment with an injectable depot neuroleptic within 1 injection interval prior to study drug administration
boolean
C2585377 (UMLS CUI [1])