ID

34162

Description

Effect of Chemotherapy on Pain Sensitivity and Patient-reported Symptoms; ODM derived from: https://clinicaltrials.gov/show/NCT01983982

Lien

https://clinicaltrials.gov/show/NCT01983982

Mots-clés

  1. 14/01/2019 14/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

14 janvier 2019

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 Cancer NCT01983982

Eligibility Breast Cancer NCT01983982

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
female gender
Description

ID.1

Type de données

boolean

histologically proven stage i-iii invasive carcinoma of the breast who is planning to receive a standard dose of adjuvant chemotherapy.
Description

ID.2

Type de données

boolean

surgical resection should be complete at the time of study enrollment.
Description

ID.3

Type de données

boolean

eastern cooperative oncology group performance status 0-2.
Description

ID.4

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
average pain over the past 24 hours of 4 or greater on a 0-10 scale.
Description

ID.5

Type de données

boolean

peripheral sensory neuropathy grade 2 or higher.
Description

ID.6

Type de données

boolean

personal history of schizophrenia or major depressive disorder, or history of suicidal ideation or attempt within the past 2 years.
Description

ID.7

Type de données

boolean

thumbnail abnormalities on either hand (such as artificial nails) that are likely to alter pain perception during testing.
Description

ID.8

Type de données

boolean

pregnant or nursing.
Description

ID.9

Type de données

boolean

no prior chemotherapy for any reason
Description

ID.10

Type de données

boolean

Similar models

Eligibility Breast Cancer NCT01983982

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
female gender
boolean
ID.2
Item
histologically proven stage i-iii invasive carcinoma of the breast who is planning to receive a standard dose of adjuvant chemotherapy.
boolean
ID.3
Item
surgical resection should be complete at the time of study enrollment.
boolean
ID.4
Item
eastern cooperative oncology group performance status 0-2.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
average pain over the past 24 hours of 4 or greater on a 0-10 scale.
boolean
ID.6
Item
peripheral sensory neuropathy grade 2 or higher.
boolean
ID.7
Item
personal history of schizophrenia or major depressive disorder, or history of suicidal ideation or attempt within the past 2 years.
boolean
ID.8
Item
thumbnail abnormalities on either hand (such as artificial nails) that are likely to alter pain perception during testing.
boolean
ID.9
Item
pregnant or nursing.
boolean
ID.10
Item
no prior chemotherapy for any reason
boolean

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