ID

22014

Beskrivning

IRIS Followed by mFOLFOX6 or the Reverse Sequence in Advanced Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00316745

Länk

https://clinicaltrials.gov/show/NCT00316745

Nyckelord

Versioner (1)
  1. 2017-05-14 2017-05-14 -
Uppladdad den

14 maj 2017

DOI

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Creative Commons BY 4.0
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Eligibility Metastatic Colorectal Cancer NCT00316745

Engelsk

Eligibility Metastatic Colorectal Cancer NCT00316745

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
1) histological diagnosis of colorectal cancer.
Beskrivning

colorectal cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C0009402
2） age: 18 - 75 years.
Beskrivning

age

Datatyp

text

Alias
UMLS CUI [1]
C0001779
3） no prior chemotherapy
Beskrivning

prior chemotherapy

Datatyp

text

Alias
UMLS CUI [1]
C1514457
4） ecog performance status 0 to 2
Beskrivning

ecog

Datatyp

text

Alias
UMLS CUI [1]
C1520224
5) a life expectancy of at least 3 months
Beskrivning

life expectancy

Datatyp

text

Alias
UMLS CUI [1]
C0023671
6) adequate function of major organs (bone marrow, heart, lungs, liver etc.). wbc ≧3,500/mm3 and neutrophil ≧2,000/mm3. hb ≧10.0 g/dl. platelet count ≧100,000/mm3. ast and alt ≦2.5 times the upper limit of normal (excluding liver metastasis). t-bil ≦1.5 mg/dl. creatinine ≦1.5 mg/ dl.
Beskrivning

organ function, hematologic, hepatic, renal function

Datatyp

text

Alias
UMLS CUI [1]
C0678852
UMLS CUI [2,1]
C0221130
UMLS CUI [2,2]
C0023508
UMLS CUI [2,3]
C0948762
UMLS CUI [2,4]
C0019046
UMLS CUI [2,5]
C0005821
UMLS CUI [3,1]
C0232741
UMLS CUI [3,2]
C1278039
UMLS CUI [3,3]
C0201899
UMLS CUI [3,4]
C0201836
UMLS CUI [4,1]
C0232804
UMLS CUI [4,2]
C0201976
7) patients must have the ability to understand and the willingness to sign a written informed contact document.
Beskrivning

informed consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patients receiving blood transfusion, blood derivatives or granulocyte-colony stimulating factor within 7days prior to entering the study.
Beskrivning

blood products, granulocyte colony stimulating factor

Datatyp

boolean

Alias
UMLS CUI [1]
C0456388
UMLS CUI [2]
C0079459
2. patients can not have oral intake
Beskrivning

oral intake

Datatyp

boolean

Alias
UMLS CUI [1]
C0518037
3. patients receiving flucytosine treatment
Beskrivning

flucytosine

Datatyp

boolean

Alias
UMLS CUI [1]
C0016278
4. patients with severe pleural effusion or ascites.
Beskrivning

pleural effusion, ascites

Datatyp

boolean

Alias
UMLS CUI [1]
C0032227
UMLS CUI [2]
C0003962
5. patients who have brown brain metastasis
Beskrivning

brain metastasis

Datatyp

boolean

Alias
UMLS CUI [1]
C0220650
6. patients with diarrhea 4 or more times per day
Beskrivning

diarrhea

Datatyp

boolean

Alias
UMLS CUI [1]
C0011991
7. patients with active gastrointestinal bleeding.
Beskrivning

gastrointestinal bleeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0017181
8. patients with intestinal obstruction
Beskrivning

intestinal obstruction

Datatyp

boolean

Alias
UMLS CUI [1]
C0021843
9. patients with active infection.
Beskrivning

active infection

Datatyp

boolean

Alias
UMLS CUI [1]
C0009450
10. patients with serious pulmonary disease (such as interstitial pneumonia, pulmonary fibrosis, pulmonary emphysema)
Beskrivning

pulmonary disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0024115
11. patients with serious complications (such as intestinal paralysis, intestinal obstruction, interstitial pneumonia or pulmonary fibrosis, uncontrolled diabetes mellitus, heart failure, renal failure, or hepatic failure).
Beskrivning

serious complications

Datatyp

boolean

Alias
UMLS CUI [1]
C0009566
12. patients with significant cardiac disease.
Beskrivning

cardiac disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0018799
13. patients with active multiple cancer.
Beskrivning

multiple cancer

Datatyp

boolean

Alias
UMLS CUI [1]
C0346429
14. patients with neuropathy ≥ grade 2
Beskrivning

neuropathy

Datatyp

boolean

Alias
UMLS CUI [1]
C0442874
15. patients who are pregnant, are of childbearing potential, or breast-feeding.
Beskrivning

pregnancy, childbearing potential, breast feeding

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C3831118
UMLS CUI [3]
C0006147
16. patients with severe mental disorder.
Beskrivning

mental disorder

Datatyp

boolean

Alias
UMLS CUI [1]
C0004936
17. patients with a history of serious allergic reaction.
Beskrivning

allergic reaction

Datatyp

boolean

Alias
UMLS CUI [1]
C1527304
18. judged to be ineligible for this protocol by the investigation.
Beskrivning

ineligibility by investigation

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0220825
UMLS CUI [1,2]
C1512714
Tillbaka till toppen

Similar models

Eligibility Metastatic Colorectal Cancer NCT00316745

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
colorectal cancer
Item
1) histological diagnosis of colorectal cancer.
boolean
C0009402 (UMLS CUI [1])
age
Item
2） age: 18 - 75 years.
text
C0001779 (UMLS CUI [1])
prior chemotherapy
Item
3） no prior chemotherapy
text
C1514457 (UMLS CUI [1])
ecog
Item
4） ecog performance status 0 to 2
text
C1520224 (UMLS CUI [1])
life expectancy
Item
5) a life expectancy of at least 3 months
text
C0023671 (UMLS CUI [1])
organ function, hematologic, hepatic, renal function
Item
6) adequate function of major organs (bone marrow, heart, lungs, liver etc.). wbc ≧3,500/mm3 and neutrophil ≧2,000/mm3. hb ≧10.0 g/dl. platelet count ≧100,000/mm3. ast and alt ≦2.5 times the upper limit of normal (excluding liver metastasis). t-bil ≦1.5 mg/dl. creatinine ≦1.5 mg/ dl.
text
C0678852 (UMLS CUI [1])
C0221130 (UMLS CUI [2,1])
C0023508 (UMLS CUI [2,2])
C0948762 (UMLS CUI [2,3])
C0019046 (UMLS CUI [2,4])
C0005821 (UMLS CUI [2,5])
C0232741 (UMLS CUI [3,1])
C1278039 (UMLS CUI [3,2])
C0201899 (UMLS CUI [3,3])
C0201836 (UMLS CUI [3,4])
C0232804 (UMLS CUI [4,1])
C0201976 (UMLS CUI [4,2])
informed consent
Item
7) patients must have the ability to understand and the willingness to sign a written informed contact document.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
blood products, granulocyte colony stimulating factor
Item
1. patients receiving blood transfusion, blood derivatives or granulocyte-colony stimulating factor within 7days prior to entering the study.
boolean
C0456388 (UMLS CUI [1])
C0079459 (UMLS CUI [2])
oral intake
Item
2. patients can not have oral intake
boolean
C0518037 (UMLS CUI [1])
flucytosine
Item
3. patients receiving flucytosine treatment
boolean
C0016278 (UMLS CUI [1])
pleural effusion, ascites
Item
4. patients with severe pleural effusion or ascites.
boolean
C0032227 (UMLS CUI [1])
C0003962 (UMLS CUI [2])
brain metastasis
Item
5. patients who have brown brain metastasis
boolean
C0220650 (UMLS CUI [1])
diarrhea
Item
6. patients with diarrhea 4 or more times per day
boolean
C0011991 (UMLS CUI [1])
gastrointestinal bleeding
Item
7. patients with active gastrointestinal bleeding.
boolean
C0017181 (UMLS CUI [1])
intestinal obstruction
Item
8. patients with intestinal obstruction
boolean
C0021843 (UMLS CUI [1])
active infection
Item
9. patients with active infection.
boolean
C0009450 (UMLS CUI [1])
pulmonary disease
Item
10. patients with serious pulmonary disease (such as interstitial pneumonia, pulmonary fibrosis, pulmonary emphysema)
boolean
C0024115 (UMLS CUI [1])
serious complications
Item
11. patients with serious complications (such as intestinal paralysis, intestinal obstruction, interstitial pneumonia or pulmonary fibrosis, uncontrolled diabetes mellitus, heart failure, renal failure, or hepatic failure).
boolean
C0009566 (UMLS CUI [1])
cardiac disease
Item
12. patients with significant cardiac disease.
boolean
C0018799 (UMLS CUI [1])
multiple cancer
Item
13. patients with active multiple cancer.
boolean
C0346429 (UMLS CUI [1])
neuropathy
Item
14. patients with neuropathy ≥ grade 2
boolean
C0442874 (UMLS CUI [1])
pregnancy, childbearing potential, breast feeding
Item
15. patients who are pregnant, are of childbearing potential, or breast-feeding.
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
mental disorder
Item
16. patients with severe mental disorder.
boolean
C0004936 (UMLS CUI [1])
allergic reaction
Item
17. patients with a history of serious allergic reaction.
boolean
C1527304 (UMLS CUI [1])
ineligibility by investigation
Item
18. judged to be ineligible for this protocol by the investigation.
boolean
C0220825 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
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