ID

13147

Description

Preoperative or Postoperative Therapy of Patients With Stages IB, II, IIIA Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00193310

Lien

https://clinicaltrials.gov/show/NCT00193310

Mots-clés

  1. 19/01/2016 19/01/2016 -
Téléchargé le

19 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Lung Cancer NCT00193310

Eligibility Lung Cancer NCT00193310

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
non-small cell lung cancer
Description

non-small cell lung cancer

Type de données

boolean

Alias
UMLS CUI [1]
C0007131
neoadjuvant candidates must have potentially resectable disease
Description

neoadjuvant therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0600558
UMLS CUI [2]
C0015250
adjuvant candidates must have had complete resection
Description

adjuvant therapy

Type de données

boolean

Alias
UMLS CUI [1]
C0677850
UMLS CUI [2]
C0015250
clinical stage ib, ii, or iiia non-small cell lung cancer
Description

tumor stage

Type de données

boolean

Alias
UMLS CUI [1]
C1300072
ecog performance status 0 or 1
Description

ecog

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
adequate bone marrow, liver and kidney function
Description

bone marrow, liver and kidney function

Type de données

boolean

Alias
UMLS CUI [1]
C0232741
UMLS CUI [2]
C0005953
UMLS CUI [3]
C0232804
no previous chemotherapy or radiation therapy for non-small cell lung cancer.
Description

chemotherapy, radiotherapy

Type de données

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1522449
give written informed consent.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
stage iiia with n2 nodes > 6 cm
Description

tumor stage

Type de données

boolean

Alias
UMLS CUI [1]
C1300072
stage iiib or iv disease
Description

tumor stage

Type de données

boolean

Alias
UMLS CUI [1]
C1300072
age <18 years
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
ecog performance status 2 or higher
Description

ecog

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
considered inoperable based on general medical condition
Description

health status, inoperable

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018759
UMLS CUI [1,2]
C0205187
history of prior malignancy within five years
Description

malignancy

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
women who are pregnant or lactating
Description

pregnancy, lactation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
Description

additional criteria

Type de données

text

Similar models

Eligibility Lung Cancer NCT00193310

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
non-small cell lung cancer
Item
non-small cell lung cancer
boolean
C0007131 (UMLS CUI [1])
neoadjuvant therapy
Item
neoadjuvant candidates must have potentially resectable disease
boolean
C0600558 (UMLS CUI [1])
C0015250 (UMLS CUI [2])
adjuvant therapy
Item
adjuvant candidates must have had complete resection
boolean
C0677850 (UMLS CUI [1])
C0015250 (UMLS CUI [2])
tumor stage
Item
clinical stage ib, ii, or iiia non-small cell lung cancer
boolean
C1300072 (UMLS CUI [1])
ecog
Item
ecog performance status 0 or 1
boolean
C1520224 (UMLS CUI [1])
bone marrow, liver and kidney function
Item
adequate bone marrow, liver and kidney function
boolean
C0232741 (UMLS CUI [1])
C0005953 (UMLS CUI [2])
C0232804 (UMLS CUI [3])
chemotherapy, radiotherapy
Item
no previous chemotherapy or radiation therapy for non-small cell lung cancer.
boolean
C0392920 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])
informed consent
Item
give written informed consent.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
tumor stage
Item
stage iiia with n2 nodes > 6 cm
boolean
C1300072 (UMLS CUI [1])
tumor stage
Item
stage iiib or iv disease
boolean
C1300072 (UMLS CUI [1])
age
Item
age <18 years
boolean
C0001779 (UMLS CUI [1])
ecog
Item
ecog performance status 2 or higher
boolean
C1520224 (UMLS CUI [1])
health status, inoperable
Item
considered inoperable based on general medical condition
boolean
C0018759 (UMLS CUI [1,1])
C0205187 (UMLS CUI [1,2])
malignancy
Item
history of prior malignancy within five years
boolean
C0006826 (UMLS CUI [1])
pregnancy, lactation
Item
women who are pregnant or lactating
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
additional criteria
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have.
text

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