ID

35360

Beschrijving

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

Trefwoorden

Versies (1)
  1. 02-03-19 02-03-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

2 maart 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Colorectal Cancer NCT02202928

Engels

Eligibility Colorectal Cancer NCT02202928

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
18~80 years old;
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
histologically confirmed with colorectal cancer at stage ⅰ~ⅲ;
Beschrijving

Colorectal Carcinoma TNM clinical staging

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009402
UMLS CUI [1,2]
C3258246
patients who can accept curative operations;
Beschrijving

Curative Surgery Accepting

Datatype

boolean

Alias
UMLS CUI [1,1]
C1511562
UMLS CUI [1,2]
C1272684
patients who have a life expectancy of at least 3 months;
Beschrijving

Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
eastern cooperative oncology group (ecog) performance status was 0 - 1.
Beschrijving

ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
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 ;
Beschrijving

Hemoglobin measurement | Platelet Count measurement | Alanine aminotransferase increased | Aspartate aminotransferase increased | Blood urea increased | Serum creatinine raised

Datatype

boolean

Alias
UMLS CUI [1]
C0518015
UMLS CUI [2]
C0032181
UMLS CUI [3]
C0151905
UMLS CUI [4]
C0151904
UMLS CUI [5]
C0151539
UMLS CUI [6]
C0700225
known or suspected allergy to the investigational agent or any agent given in association with this trial;
Beschrijving

Hypersensitivity Investigational New Drug | Hypersensitivity Clinical Trial Drug

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0008976
UMLS CUI [2,3]
C0013227
pregnant or lactating patients;
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
known history of human immunodeficiency virus (hiv), hepatitis c virus (hcv) or treponemapallidun (tp) infection;
Beschrijving

HIV Infection | Hepatitis C | Treponema pallidum infection

Datatype

boolean

Alias
UMLS CUI [1]
C0019693
UMLS CUI [2]
C0019196
UMLS CUI [3]
C0039128
patients who are suffering from serious autoimmune disease;
Beschrijving

Autoimmune Disease Serious

Datatype

boolean

Alias
UMLS CUI [1,1]
C0004364
UMLS CUI [1,2]
C0205404
history of organ allograft;
Beschrijving

Organ allograft

Datatype

boolean

Alias
UMLS CUI [1,1]
C0178784
UMLS CUI [1,2]
C0040739
patients who had distant metastases;
Beschrijving

Distant metastasis

Datatype

boolean

Alias
UMLS CUI [1]
C1269798
patients who had active infection;
Beschrijving

Communicable Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
prior use of any anti-cancer treatment in 30 days;
Beschrijving

Cancer treatment

Datatype

boolean

Alias
UMLS CUI [1]
C0920425
now or recently will join another experimental clinical study ;
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
other situations that the researchers considered unsuitable for this study.
Beschrijving

Social situation Study Subject Participation Status Inappropriate

Datatype

boolean

Alias
UMLS CUI [1,1]
C0748872
UMLS CUI [1,2]
C2348568
UMLS CUI [1,3]
C1548788
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Similar models

Eligibility Colorectal Cancer NCT02202928

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
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])
Curative Surgery Accepting
Item
patients who can accept curative operations;
boolean
C1511562 (UMLS CUI [1,1])
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])
Item Group
C0680251 (UMLS CUI)
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])
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])
Pregnancy | Breast Feeding
Item
pregnant or lactating patients;
boolean
C0032961 (UMLS CUI [1])
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])
Autoimmune Disease Serious
Item
patients who are suffering from serious autoimmune disease;
boolean
C0004364 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
Organ allograft
Item
history of organ allograft;
boolean
C0178784 (UMLS CUI [1,1])
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])
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