ID

17244

Description

Molecular Profiling in Lung Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00191308

Lien

https://clinicaltrials.gov/show/NCT00191308

Mots-clés

  1. 01/09/2016 01/09/2016 -
Téléchargé le

1 septembre 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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Eligibility Non-Small Cell Lung Cancer NCT00191308

Eligibility Non-Small Cell Lung Cancer NCT00191308

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologic documentation of non-small cell lung cancer (nsclc)
Description

Non-small cell lung cancer

Type de données

boolean

Alias
UMLS CUI [1]
C0007131
tumor must be accessible by bronchoscopy for tumor tissue sample collection
Description

tumor accessible by bronchoscopy for tumor tissue sample collection

Type de données

boolean

Alias
UMLS CUI [1]
C0189406
patients must have lung cancer with clinical stage ib, ii, iiia
Description

Tumor Stage

Type de données

boolean

Alias
UMLS CUI [1]
C1300072
eastern cooperative oncology group (ecog) performance status 0 or 1
Description

ECOG

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
patients must not have received prior systemic chemotherapy or radiation therapy for nsclc (prior resection of lung is allowed provided at least 5 years have elapsed between prior surgery and enrolment)
Description

Prior systemic chemotherapy or radiation therapy

Type de données

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
bronchoalveolar carcinoma or stage iiia tumor involving the superior sulcus (pancoast tumors)
Description

Pancoast tumor

Type de données

boolean

Alias
UMLS CUI [1]
C0549471
pregnant or breast feeding patients
Description

Pregnant or breast feeding

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients who have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry
Description

Investigational Drug

Type de données

boolean

Alias
UMLS CUI [1]
C0013230
patients with history or presence of other malignancy except in situ carcinoma of the skin or prior malignancy treated more than 5 years before without recurrence (excluding melanoma, breast cancer and hypernephroma)
Description

Malignancy

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
unwillingness to take folic acid or vitamin b12 supplementation
Description

unwillingness to take folic acid or vitamin b12 supplementation

Type de données

boolean

Alias
UMLS CUI [1]
C0016410
UMLS CUI [2]
C3661610

Similar models

Eligibility Non-Small Cell Lung Cancer NCT00191308

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Non-small cell lung cancer
Item
pathologic documentation of non-small cell lung cancer (nsclc)
boolean
C0007131 (UMLS CUI [1])
tumor accessible by bronchoscopy for tumor tissue sample collection
Item
tumor must be accessible by bronchoscopy for tumor tissue sample collection
boolean
C0189406 (UMLS CUI [1])
Tumor Stage
Item
patients must have lung cancer with clinical stage ib, ii, iiia
boolean
C1300072 (UMLS CUI [1])
ECOG
Item
eastern cooperative oncology group (ecog) performance status 0 or 1
boolean
C1520224 (UMLS CUI [1])
Prior systemic chemotherapy or radiation therapy
Item
patients must not have received prior systemic chemotherapy or radiation therapy for nsclc (prior resection of lung is allowed provided at least 5 years have elapsed between prior surgery and enrolment)
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Pancoast tumor
Item
bronchoalveolar carcinoma or stage iiia tumor involving the superior sulcus (pancoast tumors)
boolean
C0549471 (UMLS CUI [1])
Pregnant or breast feeding
Item
pregnant or breast feeding patients
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Investigational Drug
Item
patients who have received treatment within the last 30 days with a drug that has not received regulatory approval for any indication at the time of study entry
boolean
C0013230 (UMLS CUI [1])
Malignancy
Item
patients with history or presence of other malignancy except in situ carcinoma of the skin or prior malignancy treated more than 5 years before without recurrence (excluding melanoma, breast cancer and hypernephroma)
boolean
C0006826 (UMLS CUI [1])
unwillingness to take folic acid or vitamin b12 supplementation
Item
unwillingness to take folic acid or vitamin b12 supplementation
boolean
C0016410 (UMLS CUI [1])
C3661610 (UMLS CUI [2])

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