ID

32304

Beschrijving

A Randomized, Double-blind, Comparison of the Efficacy and Safety of Amisulpride Versus Low-dose Amisulpride Plus Low-dose Sulpiride in the Treatment of Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT01615185

Link

https://clinicaltrials.gov/show/NCT01615185

Trefwoorden

  1. 26-10-18 26-10-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

26 oktober 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Schizophrenia NCT01615185

Eligibility Schizophrenia NCT01615185

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
schizophrenia
Beschrijving

Schizophrenia

Datatype

boolean

Alias
UMLS CUI [1]
C0036341
cgi >=4
Beschrijving

Clinical global impression scale

Datatype

boolean

Alias
UMLS CUI [1]
C3639708
washout of antipsychotics at least 3-5 days
Beschrijving

Washout Period Antipsychotic Agents

Datatype

boolean

Alias
UMLS CUI [1,1]
C1710661
UMLS CUI [1,2]
C0040615
written informed consents
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of serious adverse events to sulpiride or amisulpride
Beschrijving

Adverse event Serious Sulpiride | Adverse event Serious Amisulpride

Datatype

boolean

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0038803
UMLS CUI [2,1]
C0877248
UMLS CUI [2,2]
C0205404
UMLS CUI [2,3]
C0103045
history of neuroleptic malignant syndrome or tardive dyskinesia to antipsychotics
Beschrijving

Neuroleptic Malignant Syndrome | Tardive Dyskinesia | Antipsychotic Agents

Datatype

boolean

Alias
UMLS CUI [1]
C0027849
UMLS CUI [2]
C0686347
UMLS CUI [3]
C0040615
treatment-resistant schizophrenia
Beschrijving

Refractory schizophrenia

Datatype

boolean

Alias
UMLS CUI [1]
C2063865
long-acting antipsychotics in the past 3 months
Beschrijving

Injection of depot antipsychotic agent

Datatype

boolean

Alias
UMLS CUI [1]
C2585377
comorbid with substance abuse/dependence
Beschrijving

Comorbidity | Substance Use Disorders | Substance Dependence

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
UMLS CUI [2]
C0038586
UMLS CUI [3]
C0038580
female subjects with pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
severe physical illness
Beschrijving

Physical illness Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0683323
UMLS CUI [1,2]
C0205082

Similar models

Eligibility Schizophrenia NCT01615185

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Schizophrenia
Item
schizophrenia
boolean
C0036341 (UMLS CUI [1])
Clinical global impression scale
Item
cgi >=4
boolean
C3639708 (UMLS CUI [1])
Washout Period Antipsychotic Agents
Item
washout of antipsychotics at least 3-5 days
boolean
C1710661 (UMLS CUI [1,1])
C0040615 (UMLS CUI [1,2])
Informed Consent
Item
written informed consents
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Adverse event Serious Sulpiride | Adverse event Serious Amisulpride
Item
history of serious adverse events to sulpiride or amisulpride
boolean
C0877248 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0038803 (UMLS CUI [1,3])
C0877248 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0103045 (UMLS CUI [2,3])
Neuroleptic Malignant Syndrome | Tardive Dyskinesia | Antipsychotic Agents
Item
history of neuroleptic malignant syndrome or tardive dyskinesia to antipsychotics
boolean
C0027849 (UMLS CUI [1])
C0686347 (UMLS CUI [2])
C0040615 (UMLS CUI [3])
Refractory schizophrenia
Item
treatment-resistant schizophrenia
boolean
C2063865 (UMLS CUI [1])
Injection of depot antipsychotic agent
Item
long-acting antipsychotics in the past 3 months
boolean
C2585377 (UMLS CUI [1])
Comorbidity | Substance Use Disorders | Substance Dependence
Item
comorbid with substance abuse/dependence
boolean
C0009488 (UMLS CUI [1])
C0038586 (UMLS CUI [2])
C0038580 (UMLS CUI [3])
Pregnancy
Item
female subjects with pregnancy
boolean
C0032961 (UMLS CUI [1])
Physical illness Severe
Item
severe physical illness
boolean
C0683323 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])

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