ID

18742

Description

The Effect of Switching to Aripiprazole on Heart Health in Overweight and Obese Patients With Schizophrenia; ODM derived from: https://clinicaltrials.gov/show/NCT00222833

Lien

https://clinicaltrials.gov/show/NCT00222833

Mots-clés

Versions (1)
  1. 18/11/2016 18/11/2016 -
Téléchargé le

18 novembre 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Overweight NCT00222833

Anglais

Eligibility Overweight NCT00222833

1 Formulaires  
  1. StudyEvent: Eligibility
    1. Eligibility Overweight NCT00222833
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female subjects ages 18-65 years
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
outpatients and stable partial hospital patients
Description

Outpatients | Hospital patients Partial Stable

Type de données

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2,1]
C0021562
UMLS CUI [2,2]
C0728938
UMLS CUI [2,3]
C0205360
diagnostic and statistical manual of mental disorders, fourth edition, text revision (dsm-iv-tr) diagnosis of schizophrenia or schizoaffective disorder
Description

Schizophrenia | Schizoaffective Disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0036341
UMLS CUI [2]
C0036337
no psychiatric hospitalization in 30 days prior to study start
Description

psychiatric hospitalization

Type de données

boolean

Alias
UMLS CUI [1]
C0748061
partially remitted patients with a panss score below 100 at screening
Description

Patient in partial remission | Positive and negative syndrome scale

Type de données

boolean

Alias
UMLS CUI [1]
C1562651
UMLS CUI [2]
C0451383
currently on a stable dose of only one antipsychotic for at least 30 days prior to study start
Description

Antipsychotic Agent Singular Dose Stable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0040615
UMLS CUI [1,2]
C0205171
UMLS CUI [1,3]
C0178602
UMLS CUI [1,4]
C0205360
currently receiving a stable dose of all other psychotropic medications for at least 30 days prior to study start
Description

Psychotropic Drugs Dose Stable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0033978
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
bmi greater than 26
Description

Body mass index

Type de données

boolean

Alias
UMLS CUI [1]
C1305855
female patients of childbearing age must be using an acceptable method of birth control for at least 1 month prior to participation in the research study and continue for at least 4 weeks after the final study visit.
Description

Childbearing Potential Contraceptive methods

Type de données

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
ability to provide informed consent.
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
mental retardation
Description

Mental Retardation

Type de données

boolean

Alias
UMLS CUI [1]
C0025362
current treatment with clozapine
Description

Clozapine

Type de données

boolean

Alias
UMLS CUI [1]
C0009079
currently enrolled in a weight management program or receiving pharmacological treatment for weight reduction
Description

Weight Reduction Program | Weight reduction regimen pharmacological

Type de données

boolean

Alias
UMLS CUI [1]
C3179079
UMLS CUI [2,1]
C0311130
UMLS CUI [2,2]
C0205464
serious or unstable medical illness
Description

Illness Serious | Illness Unstable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0221423
UMLS CUI [1,2]
C0205404
UMLS CUI [2,1]
C0221423
UMLS CUI [2,2]
C0443343
female patients who are pregnant, lactating, or plan to become pregnant during the study period
Description

Pregnancy | Breast Feeding | Pregnancy, Planned

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
concurrently receiving treatment with ketoconazole, quinidine, carbamazepine.
Description

Ketoconazole | Quinidine | Carbamazepine

Type de données

boolean

Alias
UMLS CUI [1]
C0022625
UMLS CUI [2]
C0034414
UMLS CUI [3]
C0006949
Retour au début de la page

Similar models

Eligibility Overweight NCT00222833

1 Formulaires
  1. StudyEvent: Eligibility
    1. Eligibility Overweight NCT00222833
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
male and female subjects ages 18-65 years
boolean
C0001779 (UMLS CUI [1])
Outpatients | Hospital patients Partial Stable
Item
outpatients and stable partial hospital patients
boolean
C0029921 (UMLS CUI [1])
C0021562 (UMLS CUI [2,1])
C0728938 (UMLS CUI [2,2])
C0205360 (UMLS CUI [2,3])
Schizophrenia | Schizoaffective Disorder
Item
diagnostic and statistical manual of mental disorders, fourth edition, text revision (dsm-iv-tr) diagnosis of schizophrenia or schizoaffective disorder
boolean
C0036341 (UMLS CUI [1])
C0036337 (UMLS CUI [2])
psychiatric hospitalization
Item
no psychiatric hospitalization in 30 days prior to study start
boolean
C0748061 (UMLS CUI [1])
Patient in partial remission | Positive and negative syndrome scale
Item
partially remitted patients with a panss score below 100 at screening
boolean
C1562651 (UMLS CUI [1])
C0451383 (UMLS CUI [2])
Antipsychotic Agent Singular Dose Stable
Item
currently on a stable dose of only one antipsychotic for at least 30 days prior to study start
boolean
C0040615 (UMLS CUI [1,1])
C0205171 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0205360 (UMLS CUI [1,4])
Psychotropic Drugs Dose Stable
Item
currently receiving a stable dose of all other psychotropic medications for at least 30 days prior to study start
boolean
C0033978 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
Body mass index
Item
bmi greater than 26
boolean
C1305855 (UMLS CUI [1])
Childbearing Potential Contraceptive methods
Item
female patients of childbearing age must be using an acceptable method of birth control for at least 1 month prior to participation in the research study and continue for at least 4 weeks after the final study visit.
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Informed Consent
Item
ability to provide informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Mental Retardation
Item
mental retardation
boolean
C0025362 (UMLS CUI [1])
Clozapine
Item
current treatment with clozapine
boolean
C0009079 (UMLS CUI [1])
Weight Reduction Program | Weight reduction regimen pharmacological
Item
currently enrolled in a weight management program or receiving pharmacological treatment for weight reduction
boolean
C3179079 (UMLS CUI [1])
C0311130 (UMLS CUI [2,1])
C0205464 (UMLS CUI [2,2])
Illness Serious | Illness Unstable
Item
serious or unstable medical illness
boolean
C0221423 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0221423 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female patients who are pregnant, lactating, or plan to become pregnant during the study period
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Ketoconazole | Quinidine | Carbamazepine
Item
concurrently receiving treatment with ketoconazole, quinidine, carbamazepine.
boolean
C0022625 (UMLS CUI [1])
C0034414 (UMLS CUI [2])
C0006949 (UMLS CUI [3])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial