ID

32007

Description

Zotepine Versus Risperidone in Aggressive Schizophrenic Patients of Acute Ward; ODM derived from: https://clinicaltrials.gov/show/NCT00418873

Link

https://clinicaltrials.gov/show/NCT00418873

Keywords

Versions (1)
  1. 10/11/18 10/11/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

October 11, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Schizophrenia NCT00418873

English

Eligibility Schizophrenia NCT00418873

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18 to 65 years, male or female
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
in-patients suffering from schizophrenia according to dsm-iv diagnostic criteria with panss total score of greater than or equal to 60.
Description

Inpatient | Schizophrenia PANSS score

Data type

boolean

Alias
UMLS CUI [1]
C0021562
UMLS CUI [2,1]
C0036341
UMLS CUI [2,2]
C0451383
patients with panss-ec total score of greater than or equal to 14 and with at least one panss-ec symptom score greater than or equal to 4
Description

PANSS - Excitement

Data type

boolean

Alias
UMLS CUI [1]
C4086693
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with history of seizure or with alcohol or substance abuse in the last 6 months
Description

Seizure | Substance Use Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0036572
UMLS CUI [2]
C0038586
diabetes, parkinson's disease or phaeochromocytoma
Description

Diabetes Mellitus | Parkinson Disease | Pheochromocytoma

Data type

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2]
C0030567
UMLS CUI [3]
C0031511
patients with hypertension and current use of antihypertensive agents
Description

Hypertensive disease | Antihypertensive Agents

Data type

boolean

Alias
UMLS CUI [1]
C0020538
UMLS CUI [2]
C0003364
women who are pregnant, lactating or intend to become pregnant during the study period
Description

Pregnancy | Breast Feeding | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
poor response to two different antipsychotics in full dose and full course or use of clozapine previously
Description

Antipsychotic Agents Different Quantity | Clozapine | Poor response to treatment

Data type

boolean

Alias
UMLS CUI [1,1]
C0040615
UMLS CUI [1,2]
C1705242
UMLS CUI [1,3]
C1265611
UMLS CUI [2]
C0009079
UMLS CUI [3]
C1320680
renal, hepatic, haematologic disease or other conditions may not suitable for the study based on investigator's evaluation
Description

Kidney Disease Study Subject Participation Status Inappropriate | Liver disease Study Subject Participation Status Inappropriate | Hematological Disease Study Subject Participation Status Inappropriate | Other medical condition Study Subject Participation Status Inappropriate

Data type

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C1548788
UMLS CUI [2,1]
C0023895
UMLS CUI [2,2]
C2348568
UMLS CUI [2,3]
C1548788
UMLS CUI [3,1]
C0018939
UMLS CUI [3,2]
C2348568
UMLS CUI [3,3]
C1548788
UMLS CUI [4,1]
C3843040
UMLS CUI [4,2]
C2348568
UMLS CUI [4,3]
C1548788
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Similar models

Eligibility Schizophrenia NCT00418873

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
aged 18 to 65 years, male or female
boolean
C0001779 (UMLS CUI [1])
Inpatient | Schizophrenia PANSS score
Item
in-patients suffering from schizophrenia according to dsm-iv diagnostic criteria with panss total score of greater than or equal to 60.
boolean
C0021562 (UMLS CUI [1])
C0036341 (UMLS CUI [2,1])
C0451383 (UMLS CUI [2,2])
PANSS - Excitement
Item
patients with panss-ec total score of greater than or equal to 14 and with at least one panss-ec symptom score greater than or equal to 4
boolean
C4086693 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Seizure | Substance Use Disorders
Item
patients with history of seizure or with alcohol or substance abuse in the last 6 months
boolean
C0036572 (UMLS CUI [1])
C0038586 (UMLS CUI [2])
Diabetes Mellitus | Parkinson Disease | Pheochromocytoma
Item
diabetes, parkinson's disease or phaeochromocytoma
boolean
C0011849 (UMLS CUI [1])
C0030567 (UMLS CUI [2])
C0031511 (UMLS CUI [3])
Hypertensive disease | Antihypertensive Agents
Item
patients with hypertension and current use of antihypertensive agents
boolean
C0020538 (UMLS CUI [1])
C0003364 (UMLS CUI [2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
women who are pregnant, lactating or intend to become pregnant during the study period
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Antipsychotic Agents Different Quantity | Clozapine | Poor response to treatment
Item
poor response to two different antipsychotics in full dose and full course or use of clozapine previously
boolean
C0040615 (UMLS CUI [1,1])
C1705242 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
C0009079 (UMLS CUI [2])
C1320680 (UMLS CUI [3])
Kidney Disease Study Subject Participation Status Inappropriate | Liver disease Study Subject Participation Status Inappropriate | Hematological Disease Study Subject Participation Status Inappropriate | Other medical condition Study Subject Participation Status Inappropriate
Item
renal, hepatic, haematologic disease or other conditions may not suitable for the study based on investigator's evaluation
boolean
C0022658 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C0023895 (UMLS CUI [2,1])
C2348568 (UMLS CUI [2,2])
C1548788 (UMLS CUI [2,3])
C0018939 (UMLS CUI [3,1])
C2348568 (UMLS CUI [3,2])
C1548788 (UMLS CUI [3,3])
C3843040 (UMLS CUI [4,1])
C2348568 (UMLS CUI [4,2])
C1548788 (UMLS CUI [4,3])
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