ID

36589

Descripción

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

Palabras clave

Versiones (1)
  1. 23/5/19 23/5/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

23 de mayo de 2019

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Non Small Cell Lung Cancer Stage III NCT02247713

Inglés

Eligibility Non Small Cell Lung Cancer Stage III NCT02247713

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
pathologically confirmed nsclc
Descripción

Non-Small Cell Lung Carcinoma

Tipo de datos

boolean

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

TNM clinical staging

Tipo de datos

boolean

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

Patient Available Follow-up

Tipo de datos

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
Descripción

Patient suitable Therapeutic procedure | Target Volume Radical

Tipo de datos

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
Descripción

ECOG performance status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1520224
signed informed consent
Descripción

Informed Consent

Tipo de datos

boolean

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

Ability Commence Therapeutic radiology procedure | Radiotherapy planning PET/CT

Tipo de datos

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)
Descripción

Patient suitable Chemoradiotherapy

Tipo de datos

boolean

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

Exclusion Criteria

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

Cancer Other | Exception Skin carcinoma

Tipo de datos

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
Descripción

TNM clinical staging

Tipo de datos

boolean

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

Informed Consent Unable

Tipo de datos

boolean

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

Diabetic - poor control

Tipo de datos

boolean

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

Pregnancy | Breast Feeding

Tipo de datos

boolean

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

Tuberculosis

Tipo de datos

boolean

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

Chemotherapy Neoadjuvant

Tipo de datos

boolean

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

Eligibility Non Small Cell Lung Cancer Stage III NCT02247713

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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