ID

38132

Description

Fat Metabolism Following Chemotherapy in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01890824

Lien

https://clinicaltrials.gov/show/NCT01890824

Mots-clés

  1. 20/09/2019 20/09/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

20 septembre 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01890824

Eligibility Breast Cancer NCT01890824

Criteria
Description

Criteria

diagnosed with breast cancer
Description

Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C0678222
scheduled for chemotherapy
Description

Chemotherapy Scheduled

Type de données

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0205539
ability to sign informed consent
Description

Informed Consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
age 30 years and older
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
ability to lie in supine position for 7 hours
Description

Ability to lie down Supine Position Duration

Type de données

boolean

Alias
UMLS CUI [1,1]
C0560840
UMLS CUI [1,2]
C0038846
UMLS CUI [1,3]
C0449238
inclusion criteria healthy subjects:
Description

Inclusion criteria Healthy Volunteers

Type de données

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C1708335
healthy male & female according to the investigator's or appointed staff's judgment
Description

Gender Healthy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C3898900
age 30 years or older
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
no diagnosis of cancer
Description

Malignant Neoplasms Absent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0332197
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
presence of fever within the last 3 days
Description

Fever

Type de données

boolean

Alias
UMLS CUI [1]
C0015967
untreated metabolic diseases including hepatic or renal disorder
Description

Metabolic Diseases Untreated | Liver disease Untreated | Kidney Disease Untreated

Type de données

boolean

Alias
UMLS CUI [1,1]
C0025517
UMLS CUI [1,2]
C0332155
UMLS CUI [2,1]
C0023895
UMLS CUI [2,2]
C0332155
UMLS CUI [3,1]
C0022658
UMLS CUI [3,2]
C0332155
presence of acute illness or metabolically unstable chronic illness
Description

Acute illness | Chronic disease Metabolic Unstable

Type de données

boolean

Alias
UMLS CUI [1]
C4061114
UMLS CUI [2,1]
C0008679
UMLS CUI [2,2]
C0311400
UMLS CUI [2,3]
C0443343
use of nutritional supplements within 5 days of first test day
Description

Dietary Supplements

Type de données

boolean

Alias
UMLS CUI [1]
C0242295
any other condition according to the pi or nurse that would interfere with the study or safety of the patient
Description

Condition Interferes with Clinical Trial | Condition Interferes with Patient safety

Type de données

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0008976
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C1113679
failure to give informed consent
Description

Informed Consent failed

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0231175
possible) pregnancy
Description

Pregnancy | Possible pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0425965

Similar models

Eligibility Breast Cancer NCT01890824

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Breast Carcinoma
Item
diagnosed with breast cancer
boolean
C0678222 (UMLS CUI [1])
Chemotherapy Scheduled
Item
scheduled for chemotherapy
boolean
C0392920 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Informed Consent
Item
ability to sign informed consent
boolean
C0021430 (UMLS CUI [1])
Age
Item
age 30 years and older
boolean
C0001779 (UMLS CUI [1])
Ability to lie down Supine Position Duration
Item
ability to lie in supine position for 7 hours
boolean
C0560840 (UMLS CUI [1,1])
C0038846 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Inclusion criteria Healthy Volunteers
Item
inclusion criteria healthy subjects:
boolean
C1512693 (UMLS CUI [1,1])
C1708335 (UMLS CUI [1,2])
Gender Healthy
Item
healthy male & female according to the investigator's or appointed staff's judgment
boolean
C0079399 (UMLS CUI [1,1])
C3898900 (UMLS CUI [1,2])
Age
Item
age 30 years or older
boolean
C0001779 (UMLS CUI [1])
Malignant Neoplasms Absent
Item
no diagnosis of cancer
boolean
C0006826 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Fever
Item
presence of fever within the last 3 days
boolean
C0015967 (UMLS CUI [1])
Metabolic Diseases Untreated | Liver disease Untreated | Kidney Disease Untreated
Item
untreated metabolic diseases including hepatic or renal disorder
boolean
C0025517 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2,1])
C0332155 (UMLS CUI [2,2])
C0022658 (UMLS CUI [3,1])
C0332155 (UMLS CUI [3,2])
Acute illness | Chronic disease Metabolic Unstable
Item
presence of acute illness or metabolically unstable chronic illness
boolean
C4061114 (UMLS CUI [1])
C0008679 (UMLS CUI [2,1])
C0311400 (UMLS CUI [2,2])
C0443343 (UMLS CUI [2,3])
Dietary Supplements
Item
use of nutritional supplements within 5 days of first test day
boolean
C0242295 (UMLS CUI [1])
Condition Interferes with Clinical Trial | Condition Interferes with Patient safety
Item
any other condition according to the pi or nurse that would interfere with the study or safety of the patient
boolean
C0348080 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C1113679 (UMLS CUI [2,3])
Informed Consent failed
Item
failure to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Pregnancy | Possible pregnancy
Item
possible) pregnancy
boolean
C0032961 (UMLS CUI [1])
C0425965 (UMLS CUI [2])

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