ID

36589

Description

An International Study on the Use of PET/CT in Radiotherapy Planning in Low and Middle Income Countries; ODM derived from: https://clinicaltrials.gov/show/NCT02247713

Link

https://clinicaltrials.gov/show/NCT02247713

Keywords

  1. 5/23/19 5/23/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 23, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Non Small Cell Lung Cancer Stage III NCT02247713

Eligibility Non Small Cell Lung Cancer Stage III NCT02247713

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologically confirmed nsclc
Description

Non-Small Cell Lung Carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C0007131
stage iii as per local diagnostic protocol or agreement of local multidisciplinary team
Description

TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1]
C3258246
available for clinical follow-up for at least 2 years
Description

Patient Available Follow-up

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0470187
UMLS CUI [1,3]
C3274571
suitable for treatment with a radical target volume in the opinion of a radiation oncologist
Description

Patient suitable Therapeutic procedure | Target Volume Radical

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3900053
UMLS CUI [1,3]
C0087111
UMLS CUI [2,1]
C1521840
UMLS CUI [2,2]
C0449468
UMLS CUI [2,3]
C0439807
ecog performance 0 or 1
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
signed informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
ability to commence radiation therapy within 4 weeks of acquisition of the rtp pet/ct
Description

Ability Commence Therapeutic radiology procedure | Radiotherapy planning PET/CT

Data type

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C3274784
UMLS CUI [1,3]
C1522449
UMLS CUI [2,1]
C0454111
UMLS CUI [2,2]
C1699633
suitable for concurrent chemoradiotherapy (prospective cohort only)
Description

Patient suitable Chemoradiotherapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3900053
UMLS CUI [1,3]
C0436307
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
other neoplasms in the last 5 years except non-melanoma skin cancer
Description

Cancer Other | Exception Skin carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C1707251
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0699893
stage iv disease diagnosed before acquisition of staging pet/ct
Description

TNM clinical staging

Data type

boolean

Alias
UMLS CUI [1]
C3258246
inability to provide informed consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
uncontrolled diabetes mellitus
Description

Diabetic - poor control

Data type

boolean

Alias
UMLS CUI [1]
C0421258
pregnant or breast feeding mothers
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
tuberculosis
Description

Tuberculosis

Data type

boolean

Alias
UMLS CUI [1]
C0041296
neo-adjuvant chemotherapy
Description

Chemotherapy Neoadjuvant

Data type

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1298676

Similar models

Eligibility Non Small Cell Lung Cancer Stage III NCT02247713

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Non-Small Cell Lung Carcinoma
Item
pathologically confirmed nsclc
boolean
C0007131 (UMLS CUI [1])
TNM clinical staging
Item
stage iii as per local diagnostic protocol or agreement of local multidisciplinary team
boolean
C3258246 (UMLS CUI [1])
Patient Available Follow-up
Item
available for clinical follow-up for at least 2 years
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C3274571 (UMLS CUI [1,3])
Patient suitable Therapeutic procedure | Target Volume Radical
Item
suitable for treatment with a radical target volume in the opinion of a radiation oncologist
boolean
C0030705 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1521840 (UMLS CUI [2,1])
C0449468 (UMLS CUI [2,2])
C0439807 (UMLS CUI [2,3])
ECOG performance status
Item
ecog performance 0 or 1
boolean
C1520224 (UMLS CUI [1])
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Ability Commence Therapeutic radiology procedure | Radiotherapy planning PET/CT
Item
ability to commence radiation therapy within 4 weeks of acquisition of the rtp pet/ct
boolean
C0085732 (UMLS CUI [1,1])
C3274784 (UMLS CUI [1,2])
C1522449 (UMLS CUI [1,3])
C0454111 (UMLS CUI [2,1])
C1699633 (UMLS CUI [2,2])
Patient suitable Chemoradiotherapy
Item
suitable for concurrent chemoradiotherapy (prospective cohort only)
boolean
C0030705 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C0436307 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Cancer Other | Exception Skin carcinoma
Item
other neoplasms in the last 5 years except non-melanoma skin cancer
boolean
C1707251 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0699893 (UMLS CUI [2,2])
TNM clinical staging
Item
stage iv disease diagnosed before acquisition of staging pet/ct
boolean
C3258246 (UMLS CUI [1])
Informed Consent Unable
Item
inability to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Diabetic - poor control
Item
uncontrolled diabetes mellitus
boolean
C0421258 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breast feeding mothers
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Tuberculosis
Item
tuberculosis
boolean
C0041296 (UMLS CUI [1])
Chemotherapy Neoadjuvant
Item
neo-adjuvant chemotherapy
boolean
C0392920 (UMLS CUI [1,1])
C1298676 (UMLS CUI [1,2])

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