Eligibility Breast Cancer NCT00772824

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patients > 18 years of age
Descrição

Age

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
histologically or cytologically proven breast cancer
Descrição

Breast Carcinoma

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0678222
receiving cef chemotherapy cycles presently or in the past
Descrição

CEF Chemotherapy cycle

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0060133
UMLS CUI [1,2]
C1302181
the patients who will give informed consent to participate in the study
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
patients must have sufficient organ and marrow function
Descrição

Organ function | Bone Marrow function

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0678852
UMLS CUI [2,1]
C0005953
UMLS CUI [2,2]
C0031843
stage 1 neuropathy, subclinical neuropathy, surgery induced neuropathy
Descrição

Neuropathy Stage | Neuropathy Subclinical | Neuropathy Surgery Induced

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0442874
UMLS CUI [1,2]
C0205563
UMLS CUI [2,1]
C0442874
UMLS CUI [2,2]
C0205211
UMLS CUI [3,1]
C0442874
UMLS CUI [3,2]
C0543467
UMLS CUI [3,3]
C0205263
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Descrição

Pregnancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
clinical/biochemical severe liver failure
Descrição

Liver Failure Severe

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0085605
UMLS CUI [1,2]
C0205082
clinical/biochemical severe renal dysfunction
Descrição

Renal dysfunction Severe

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3279454
UMLS CUI [1,2]
C0205082
refusal to participate in the study
Descrição

Study Subject Participation Status | Participation Refused

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0679823
UMLS CUI [2,2]
C1705116
patients who have received prior chemotherapy with paclitaxel.
Descrição

Paclitaxel

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0144576
patients who have neuropathy due to any known systemic or metabolic causes like diabetes, leprosy, nutritional deficiency induced (vit. b12) etc
Descrição

Neuropathy Due to Causes Systemic | Neuropathy Due to Causes Metabolic | Diabetes Mellitus | Leprosy | Malnutrition | Vitamin B 12 Deficiency

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0442874
UMLS CUI [1,2]
C0678226
UMLS CUI [1,3]
C0015127
UMLS CUI [1,4]
C0205373
UMLS CUI [2,1]
C0442874
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0015127
UMLS CUI [2,4]
C0311400
UMLS CUI [3]
C0011849
UMLS CUI [4]
C0023343
UMLS CUI [5]
C0162429
UMLS CUI [6]
C0042847

Similar models

Eligibility Breast Cancer NCT00772824

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
the patients > 18 years of age
boolean
C0001779 (UMLS CUI [1])
Breast Carcinoma
Item
histologically or cytologically proven breast cancer
boolean
C0678222 (UMLS CUI [1])
CEF Chemotherapy cycle
Item
receiving cef chemotherapy cycles presently or in the past
boolean
C0060133 (UMLS CUI [1,1])
C1302181 (UMLS CUI [1,2])
Informed Consent
Item
the patients who will give informed consent to participate in the study
boolean
C0021430 (UMLS CUI [1])
Organ function | Bone Marrow function
Item
patients must have sufficient organ and marrow function
boolean
C0678852 (UMLS CUI [1])
C0005953 (UMLS CUI [2,1])
C0031843 (UMLS CUI [2,2])
Neuropathy Stage | Neuropathy Subclinical | Neuropathy Surgery Induced
Item
stage 1 neuropathy, subclinical neuropathy, surgery induced neuropathy
boolean
C0442874 (UMLS CUI [1,1])
C0205563 (UMLS CUI [1,2])
C0442874 (UMLS CUI [2,1])
C0205211 (UMLS CUI [2,2])
C0442874 (UMLS CUI [3,1])
C0543467 (UMLS CUI [3,2])
C0205263 (UMLS CUI [3,3])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Liver Failure Severe
Item
clinical/biochemical severe liver failure
boolean
C0085605 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Renal dysfunction Severe
Item
clinical/biochemical severe renal dysfunction
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Study Subject Participation Status | Participation Refused
Item
refusal to participate in the study
boolean
C2348568 (UMLS CUI [1])
C0679823 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Paclitaxel
Item
patients who have received prior chemotherapy with paclitaxel.
boolean
C0144576 (UMLS CUI [1])
Neuropathy Due to Causes Systemic | Neuropathy Due to Causes Metabolic | Diabetes Mellitus | Leprosy | Malnutrition | Vitamin B 12 Deficiency
Item
patients who have neuropathy due to any known systemic or metabolic causes like diabetes, leprosy, nutritional deficiency induced (vit. b12) etc
boolean
C0442874 (UMLS CUI [1,1])
C0678226 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0205373 (UMLS CUI [1,4])
C0442874 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0015127 (UMLS CUI [2,3])
C0311400 (UMLS CUI [2,4])
C0011849 (UMLS CUI [3])
C0023343 (UMLS CUI [4])
C0162429 (UMLS CUI [5])
C0042847 (UMLS CUI [6])