Información:
Error:
ID
26574
Descripción
Study of the Effect of Glutamine Supplementation on Chemotherapy Induced Toxicities in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00772824
Link
https://clinicaltrials.gov/show/NCT00772824
Palabras clave
Versiones (1)
- 19/10/17 19/10/17 -
Titular de derechos de autor
See clinicaltrials.gov
Subido en
19 de octubre de 2017
DOI
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Licencia
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00772824
Eligibility Breast Cancer NCT00772824
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00772824
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
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])
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])
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])
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])
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])
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])
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])
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])
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])