ID

36589

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT02247713

Nyckelord

  1. 2019-05-23 2019-05-23 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

23 maj 2019

DOI

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Licens

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
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologically confirmed nsclc
Beskrivning

Non-Small Cell Lung Carcinoma

Datatyp

boolean

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

TNM clinical staging

Datatyp

boolean

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

Patient Available Follow-up

Datatyp

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
Beskrivning

Patient suitable Therapeutic procedure | Target Volume Radical

Datatyp

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
Beskrivning

ECOG performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
signed informed consent
Beskrivning

Informed Consent

Datatyp

boolean

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

Ability Commence Therapeutic radiology procedure | Radiotherapy planning PET/CT

Datatyp

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)
Beskrivning

Patient suitable Chemoradiotherapy

Datatyp

boolean

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

Exclusion Criteria

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

Cancer Other | Exception Skin carcinoma

Datatyp

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
Beskrivning

TNM clinical staging

Datatyp

boolean

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

Informed Consent Unable

Datatyp

boolean

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

Diabetic - poor control

Datatyp

boolean

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

Pregnancy | Breast Feeding

Datatyp

boolean

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

Tuberculosis

Datatyp

boolean

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

Chemotherapy Neoadjuvant

Datatyp

boolean

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

Similar models

Eligibility Non Small Cell Lung Cancer Stage III NCT02247713

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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