Informações:
Falhas:
ID
35360
Descrição
Adoptive Cell Therapy Plus Chemotherapy and Radiation After Surgery in Treating Patients With Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02202928
Link
https://clinicaltrials.gov/show/NCT02202928
Palavras-chave
Versões (1)
- 02/03/2019 02/03/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
2 de março de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT02202928
Eligibility Colorectal Cancer NCT02202928
- StudyEvent: Eligibility
Similar models
Eligibility Colorectal Cancer NCT02202928
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Age
Item
18~80 years old;
boolean
C0001779 (UMLS CUI [1])
Colorectal Carcinoma TNM clinical staging
Item
histologically confirmed with colorectal cancer at stage ⅰ~ⅲ;
boolean
C0009402 (UMLS CUI [1,1])
C3258246 (UMLS CUI [1,2])
C3258246 (UMLS CUI [1,2])
Curative Surgery Accepting
Item
patients who can accept curative operations;
boolean
C1511562 (UMLS CUI [1,1])
C1272684 (UMLS CUI [1,2])
C1272684 (UMLS CUI [1,2])
Life Expectancy
Item
patients who have a life expectancy of at least 3 months;
boolean
C0023671 (UMLS CUI [1])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status was 0 - 1.
boolean
C1520224 (UMLS CUI [1])
Hemoglobin measurement | Platelet Count measurement | Alanine aminotransferase increased | Aspartate aminotransferase increased | Blood urea increased | Serum creatinine raised
Item
hemoglobin＜8.0 g/dl,platelet count ＜75 x 10^9/l; alt, ast, bun and cr more than normal limits on 3.0 times ;
boolean
C0518015 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
C0151904 (UMLS CUI [4])
C0151539 (UMLS CUI [5])
C0700225 (UMLS CUI [6])
C0032181 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
C0151904 (UMLS CUI [4])
C0151539 (UMLS CUI [5])
C0700225 (UMLS CUI [6])
Hypersensitivity Investigational New Drug | Hypersensitivity Clinical Trial Drug
Item
known or suspected allergy to the investigational agent or any agent given in association with this trial;
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0013227 (UMLS CUI [2,3])
C0013230 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0013227 (UMLS CUI [2,3])
Pregnancy | Breast Feeding
Item
pregnant or lactating patients;
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
HIV Infection | Hepatitis C | Treponema pallidum infection
Item
known history of human immunodeficiency virus (hiv), hepatitis c virus (hcv) or treponemapallidun (tp) infection;
boolean
C0019693 (UMLS CUI [1])
C0019196 (UMLS CUI [2])
C0039128 (UMLS CUI [3])
C0019196 (UMLS CUI [2])
C0039128 (UMLS CUI [3])
Autoimmune Disease Serious
Item
patients who are suffering from serious autoimmune disease;
boolean
C0004364 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,2])
Organ allograft
Item
history of organ allograft;
boolean
C0178784 (UMLS CUI [1,1])
C0040739 (UMLS CUI [1,2])
C0040739 (UMLS CUI [1,2])
Distant metastasis
Item
patients who had distant metastases;
boolean
C1269798 (UMLS CUI [1])
Communicable Disease
Item
patients who had active infection;
boolean
C0009450 (UMLS CUI [1])
Cancer treatment
Item
prior use of any anti-cancer treatment in 30 days;
boolean
C0920425 (UMLS CUI [1])
Study Subject Participation Status
Item
now or recently will join another experimental clinical study ;
boolean
C2348568 (UMLS CUI [1])
Social situation Study Subject Participation Status Inappropriate
Item
other situations that the researchers considered unsuitable for this study.
boolean
C0748872 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])