ID

14882

Description

Safety and Efficacy Study of Mix Vaccine in Breast Carcinoma Patient; ODM derived from: https://clinicaltrials.gov/show/NCT02338804

Lien

https://clinicaltrials.gov/show/NCT02338804

Mots-clés

  1. 03/05/2016 03/05/2016 -
Téléchargé le

3 mai 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.

Groupe Item commentaires pour :

Item commentaires pour :

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

Eligibility Breast Neoplasms NCT02338804

Eligibility Breast Neoplasms NCT02338804

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1.patients diagnosed with breast carcinoma based on histology
Description

Breast Carcinoma Histologic

Type de données

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205462
2.evaluable lesions on imaging study
Description

Evaluable Disease Lesion | imaging studies

Type de données

boolean

Alias
UMLS CUI [1,1]
C1516986
UMLS CUI [1,2]
C0221198
UMLS CUI [2]
C1881134
3.without known immunodeficiency
Description

Immunologic Deficiency Syndromes

Type de données

boolean

Alias
UMLS CUI [1]
C0021051
4.age >18 and <80 years ago
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1.patients is unable or unwilling to sign informed consent
Description

Unable Informed Consent

Type de données

boolean

Alias
UMLS CUI [1,1]
C1299582
UMLS CUI [1,2]
C0021430
2.any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication
Description

Autoimmune Diseases Prednisone treatment | Immunosuppressive drug

Type de données

boolean

Alias
UMLS CUI [1,1]
C0004364
UMLS CUI [1,2]
C0747791
UMLS CUI [2]
C0499076
3.positive hiv and/or rpr (rapid plasma reagin)
Description

HIV Seropositivity | Positive rpr

Type de données

boolean

Alias
UMLS CUI [1]
C0019699
UMLS CUI [2]
C0240917
4.female patient who is pregnant or breast feeding
Description

Pregnancy | Breast Feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
5.patients, based on the opinion pf the investigator, should not be enrolled into this study
Description

patient not eligible | clinical research investigator

Type de données

boolean

Alias
UMLS CUI [1]
C3242266
UMLS CUI [2]
C1552025
6.prior anti-cancer vaccine or biological immunotherapy
Description

Vaccines Cancer treatment | Biological Immunotherapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0042210
UMLS CUI [1,2]
C0920425
UMLS CUI [2]
C1511146
7.allergic to any known ingredient of the mv compound
Description

Hypersensitivity Chemical Ingredients Investigational New Drug

Type de données

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0085993
UMLS CUI [1,3]
C0013230

Similar models

Eligibility Breast Neoplasms NCT02338804

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Breast Carcinoma Histologic
Item
1.patients diagnosed with breast carcinoma based on histology
boolean
C0678222 (UMLS CUI [1,1])
C0205462 (UMLS CUI [1,2])
Evaluable Disease Lesion | imaging studies
Item
2.evaluable lesions on imaging study
boolean
C1516986 (UMLS CUI [1,1])
C0221198 (UMLS CUI [1,2])
C1881134 (UMLS CUI [2])
Immunologic Deficiency Syndromes
Item
3.without known immunodeficiency
boolean
C0021051 (UMLS CUI [1])
Age
Item
4.age >18 and <80 years ago
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Unable Informed Consent
Item
1.patients is unable or unwilling to sign informed consent
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Autoimmune Diseases Prednisone treatment | Immunosuppressive drug
Item
2.any autoimmune disorder, which is currently being treated with prednisone or any other immune suppressive medication
boolean
C0004364 (UMLS CUI [1,1])
C0747791 (UMLS CUI [1,2])
C0499076 (UMLS CUI [2])
HIV Seropositivity | Positive rpr
Item
3.positive hiv and/or rpr (rapid plasma reagin)
boolean
C0019699 (UMLS CUI [1])
C0240917 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
4.female patient who is pregnant or breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
patient not eligible | clinical research investigator
Item
5.patients, based on the opinion pf the investigator, should not be enrolled into this study
boolean
C3242266 (UMLS CUI [1])
C1552025 (UMLS CUI [2])
Vaccines Cancer treatment | Biological Immunotherapy
Item
6.prior anti-cancer vaccine or biological immunotherapy
boolean
C0042210 (UMLS CUI [1,1])
C0920425 (UMLS CUI [1,2])
C1511146 (UMLS CUI [2])
Hypersensitivity Chemical Ingredients Investigational New Drug
Item
7.allergic to any known ingredient of the mv compound
boolean
C0020517 (UMLS CUI [1,1])
C0085993 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])

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

Les champs marqués d’un * sont obligatoires.

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