ID

33981

Description

A Study of Avastin (Bevacizumab) in Combination With Gemcitabine With or Without Cisplatin in First-Line Treatment of Elderly Patients With Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01077713

Link

https://clinicaltrials.gov/show/NCT01077713

Keywords

  1. 1/9/19 1/9/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 9, 2019

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Non-Squamous Non-Small Cell Lung Cancer NCT01077713

Eligibility Non-Squamous Non-Small Cell Lung Cancer NCT01077713

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, >=70 years of age;
Description

Adult | Age

Data type

boolean

Alias
UMLS CUI [1]
C0001675
UMLS CUI [2]
C0001779
inoperable, locally advanced, metastatic non-squamous non-small cell lung cancer;
Description

Metastatic Non-Squamous Non-Small Cell Lung Carcinoma Advanced Locally Inoperable

Data type

boolean

Alias
UMLS CUI [1,1]
C4288755
UMLS CUI [1,2]
C0205179
UMLS CUI [1,3]
C1517927
UMLS CUI [1,4]
C0205187
>=1 measurable lesion;
Description

Measurable lesion Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C1513041
UMLS CUI [1,2]
C1265611
ecog performance status 0-1.
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
neoadjuvant/adjuvant chemotherapy within 6 months prior to enrollment;
Description

Neoadjuvant Chemotherapy | Chemotherapy, Adjuvant

Data type

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C3665472
UMLS CUI [2]
C0085533
radical radiotherapy with curative intent within 28 days prior to enrollment;
Description

Therapeutic radiology procedure Radical Curative

Data type

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0439807
UMLS CUI [1,3]
C1276305
history of >=grade 2 hemoptysis in 3 months prior to enrollment;
Description

Hemoptysis Grade

Data type

boolean

Alias
UMLS CUI [1,1]
C0019079
UMLS CUI [1,2]
C0441800
evidence of cns metastases;
Description

CNS metastases

Data type

boolean

Alias
UMLS CUI [1]
C0686377
current or recent (within 10 days of first dose of avastin)use of aspirin (>325 mg/day)or full dose anticoagulants or thrombolytic agents for therapeutic purposes.
Description

Aspirin U/day | Anticoagulants Dose Full | Fibrinolytic Agents

Data type

boolean

Alias
UMLS CUI [1,1]
C0004057
UMLS CUI [1,2]
C0456683
UMLS CUI [2,1]
C0003280
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C0443225
UMLS CUI [3]
C0016018

Similar models

Eligibility Non-Squamous Non-Small Cell Lung Cancer NCT01077713

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Adult | Age
Item
adult patients, >=70 years of age;
boolean
C0001675 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Metastatic Non-Squamous Non-Small Cell Lung Carcinoma Advanced Locally Inoperable
Item
inoperable, locally advanced, metastatic non-squamous non-small cell lung cancer;
boolean
C4288755 (UMLS CUI [1,1])
C0205179 (UMLS CUI [1,2])
C1517927 (UMLS CUI [1,3])
C0205187 (UMLS CUI [1,4])
Measurable lesion Quantity
Item
>=1 measurable lesion;
boolean
C1513041 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
ECOG performance status
Item
ecog performance status 0-1.
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Neoadjuvant Chemotherapy | Chemotherapy, Adjuvant
Item
neoadjuvant/adjuvant chemotherapy within 6 months prior to enrollment;
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (UMLS CUI [1,2])
C0085533 (UMLS CUI [2])
Therapeutic radiology procedure Radical Curative
Item
radical radiotherapy with curative intent within 28 days prior to enrollment;
boolean
C1522449 (UMLS CUI [1,1])
C0439807 (UMLS CUI [1,2])
C1276305 (UMLS CUI [1,3])
Hemoptysis Grade
Item
history of >=grade 2 hemoptysis in 3 months prior to enrollment;
boolean
C0019079 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
CNS metastases
Item
evidence of cns metastases;
boolean
C0686377 (UMLS CUI [1])
Aspirin U/day | Anticoagulants Dose Full | Fibrinolytic Agents
Item
current or recent (within 10 days of first dose of avastin)use of aspirin (>325 mg/day)or full dose anticoagulants or thrombolytic agents for therapeutic purposes.
boolean
C0004057 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
C0003280 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0443225 (UMLS CUI [2,3])
C0016018 (UMLS CUI [3])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial