ID

12929

Descrizione

Pulsed Paclitaxel And Daily Thoracic Radiotherapy For Inoperable (Stage I/II) Or Unresectable Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00178256

collegamento

https://clinicaltrials.gov/show/NCT00178256

Keywords

versioni (1)
  1. 06/01/16 06/01/16 -
Titolare del copyright

CC BY-NC 3.0

Caricato su

6 gennaio 2016

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0
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Eligibility Carcinoma, Non-Small-Cell Lung NCT00178256

Inglese

Eligibility Carcinoma, Non-Small-Cell Lung NCT00178256

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically confirmed lung cancer, excluding small cell carcinoma
Descrizione

lung cancer

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0242379
inoperable stage i (t1-2n0) and ii (t1-2n1, t3n0) disease, or stage iiia (t3n1 andt1-3n2m0) and iiib (txn3m0, t4nxm0) diseases according to the american joint committee of cancer criteria 1998
Descrizione

tumor stage

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1300072
the primary tumor must be radiographically measurable.
Descrizione

the primary tumor must be radiographically measurable.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1302351
age > 18.
Descrizione

age

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0001779
karnofsky performance status > 70.
Descrizione

karnofsky performance status

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0206065
fev1 sufficient for patients to tolerate radiation therapy which is at the discretion of the radiation oncologist, usually > 800 ml
Descrizione

fev1 sufficient for patients to tolerate radiation therapy which is at the discretion of the radiation oncologist, usually > 800 ml

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0748133
labs: wbc > 3000; platelet count > 100,000; serum creatinine < 1.5 mg/dl or creatinine clearance >60 ml/min.
Descrizione

labs: wbc > 3000; platelet count > 100,000; serum creatinine < 1.5 mg/dl or creatinine clearance >60 ml/min.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0023508
UMLS CUI [2]
C0005821
UMLS CUI [3]
C0201976
UMLS CUI [4]
C0373595
laboratory values must be obtained < 3 weeks prior to registration.
Descrizione

laboratory values must be obtained < 3 weeks prior to registration.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0022885
a signed informed consent.
Descrizione

a signed informed consent.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
patients who failed prior chemotherapy are eligible. patients with prior radiotherapy to the chest region are eligible as long as the normal tissue tolerance is not violated by repeat radiotherapy.
Descrizione

patients who failed prior chemotherapy are eligible. patients with prior radiotherapy to the chest region are eligible as long as the normal tissue tolerance is not violated by repeat radiotherapy.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with medical contraindication to chemotherapy or radiotherapy.
Descrizione

patients with medical contraindication to chemotherapy or radiotherapy.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
patients with myocardial infarction within the preceding six months or symptomatic heart disease, including uncontrolled or unstable angina, uncontrolled congestive heart failure, and uncontrolled arrhythmia.
Descrizione

patients with myocardial infarction within the preceding six months or symptomatic heart disease, including uncontrolled or unstable angina, uncontrolled congestive heart failure, and uncontrolled arrhythmia.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0018799
women who are pregnant.
Descrizione

pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
patients with small cell carcinoma or mesothelioma
Descrizione

patients with small cell carcinoma or mesothelioma

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0262584
UMLS CUI [2]
C0025500
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Similar models

Eligibility Carcinoma, Non-Small-Cell Lung NCT00178256

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
lung cancer
Item
histologically confirmed lung cancer, excluding small cell carcinoma
boolean
C0242379 (UMLS CUI [1])
tumor stage
Item
inoperable stage i (t1-2n0) and ii (t1-2n1, t3n0) disease, or stage iiia (t3n1 andt1-3n2m0) and iiib (txn3m0, t4nxm0) diseases according to the american joint committee of cancer criteria 1998
boolean
C1300072 (UMLS CUI [1])
the primary tumor must be radiographically measurable.
Item
the primary tumor must be radiographically measurable.
boolean
C1302351 (UMLS CUI [1])
age
Item
age > 18.
boolean
C0001779 (UMLS CUI [1])
karnofsky performance status
Item
karnofsky performance status > 70.
boolean
C0206065 (UMLS CUI [1])
fev1 sufficient for patients to tolerate radiation therapy which is at the discretion of the radiation oncologist, usually > 800 ml
Item
fev1 sufficient for patients to tolerate radiation therapy which is at the discretion of the radiation oncologist, usually > 800 ml
boolean
C0748133 (UMLS CUI [1])
labs: wbc > 3000; platelet count > 100,000; serum creatinine < 1.5 mg/dl or creatinine clearance >60 ml/min.
Item
labs: wbc > 3000; platelet count > 100,000; serum creatinine < 1.5 mg/dl or creatinine clearance >60 ml/min.
boolean
C0023508 (UMLS CUI [1])
C0005821 (UMLS CUI [2])
C0201976 (UMLS CUI [3])
C0373595 (UMLS CUI [4])
laboratory values must be obtained < 3 weeks prior to registration.
Item
laboratory values must be obtained < 3 weeks prior to registration.
boolean
C0022885 (UMLS CUI [1])
a signed informed consent.
Item
a signed informed consent.
boolean
C0021430 (UMLS CUI [1])
patients who failed prior chemotherapy are eligible. patients with prior radiotherapy to the chest region are eligible as long as the normal tissue tolerance is not violated by repeat radiotherapy.
Item
patients who failed prior chemotherapy are eligible. patients with prior radiotherapy to the chest region are eligible as long as the normal tissue tolerance is not violated by repeat radiotherapy.
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
patients with medical contraindication to chemotherapy or radiotherapy.
Item
patients with medical contraindication to chemotherapy or radiotherapy.
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
patients with myocardial infarction within the preceding six months or symptomatic heart disease, including uncontrolled or unstable angina, uncontrolled congestive heart failure, and uncontrolled arrhythmia.
Item
patients with myocardial infarction within the preceding six months or symptomatic heart disease, including uncontrolled or unstable angina, uncontrolled congestive heart failure, and uncontrolled arrhythmia.
boolean
C0018799 (UMLS CUI [1])
pregnancy
Item
women who are pregnant.
boolean
C0032961 (UMLS CUI [1])
patients with small cell carcinoma or mesothelioma
Item
patients with small cell carcinoma or mesothelioma
boolean
C0262584 (UMLS CUI [1])
C0025500 (UMLS CUI [2])
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