Información:
Error:
ID
22752
Descripción
Amisulpride Augmentation Therapy for Clozapine-resistant Schizophrenic Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01105481
Link
https://clinicaltrials.gov/show/NCT01105481
Palabras clave
Versiones (1)
- 11/6/17 11/6/17 -
Subido en
11 de junio de 2017
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY 4.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Eligibility Treatment-resistant Schizophrenia NCT01105481
Eligibility Treatment-resistant Schizophrenia NCT01105481
- StudyEvent: Eligibility
Similar models
Eligibility Treatment-resistant Schizophrenia NCT01105481
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
schizophrenia dsm iv
Item
dsm-iv diagnosed schizophrenic patients;
boolean
C0036341 (UMLS CUI [1,1])
C0220952 (UMLS CUI [1,2])
C0220952 (UMLS CUI [1,2])
age
Item
age between 18 and 60;
boolean
C0001779 (UMLS CUI [1])
prior therapy non-responder
Item
before treatment with clozapine, documented treatment failure of two antipsychotics for an adequate duration of 6 weeks and in a sufficient dose of 600 mg/day of chlorpromazine equivalents;
boolean
C1514463 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0205269 (UMLS CUI [1,2])
failure to show a satisfactory clinical response to clozapine
Item
documented failure to show a satisfactory clinical response to an adequate clozapine treatment, defined as at least clozapine 300 mg/day for 3 months or a plasma drug level of 350ng/ml;
boolean
C0009079 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
C0205269 (UMLS CUI [1,2])
clinical global impression, panss
Item
at least moderately ill, defined as with a clinical global impression (cgi) greater than 4 or panss total score greater than 75;
boolean
C3639708 (UMLS CUI [1,1])
C0521117 (UMLS CUI [1,2])
C0451383 (UMLS CUI [2])
C0521117 (UMLS CUI [1,2])
C0451383 (UMLS CUI [2])
positive psychotic symptoms on panss
Item
persistent positive psychotic symptoms, with rating scores of moderate or worse on at least two of four positive symptom items (delusion, conceptual disorganization, hallucinatory behavior, and suspiciousness/persecution) on positive and negative syndrome scale (panss);
boolean
C1446409 (UMLS CUI [1,1])
C0871189 (UMLS CUI [1,2])
C0439793 (UMLS CUI [1,3])
C0451383 (UMLS CUI [1,4])
C0871189 (UMLS CUI [1,2])
C0439793 (UMLS CUI [1,3])
C0451383 (UMLS CUI [1,4])
concomitant treatment with lithium, anti-convulsants, antidepressants and other antipsychotic medication ;
Item
patients with concomitant treatment with lithium, anti-convulsants, antidepressants and other antipsychotic medication ;
boolean
C1707479 (UMLS CUI [1,1])
C0023870 (UMLS CUI [1,2])
C1707479 (UMLS CUI [2,1])
C0003286 (UMLS CUI [2,2])
C1707479 (UMLS CUI [3,1])
C0003289 (UMLS CUI [3,2])
C1707479 (UMLS CUI [4,1])
C0040615 (UMLS CUI [4,2])
C0023870 (UMLS CUI [1,2])
C1707479 (UMLS CUI [2,1])
C0003286 (UMLS CUI [2,2])
C1707479 (UMLS CUI [3,1])
C0003289 (UMLS CUI [3,2])
C1707479 (UMLS CUI [4,1])
C0040615 (UMLS CUI [4,2])
severe comorbidity, cardiovascular disease, cerebrovascular disease, bone marrow suppression, epilepsy
Item
patients with underlying severe medical illness, such as cardiovascular disease, cerebrovascular disease, bone marrow suppression or epilepsy;
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2])
C0007820 (UMLS CUI [3])
C0280962 (UMLS CUI [4])
C0014544 (UMLS CUI [5])
C0205082 (UMLS CUI [1,2])
C0007222 (UMLS CUI [2])
C0007820 (UMLS CUI [3])
C0280962 (UMLS CUI [4])
C0014544 (UMLS CUI [5])
substance use disorder
Item
patients with comorbid diagnosis of substance dependence;
boolean
C0038586 (UMLS CUI [1])