Informações:
Falhas:
ID
41136
Descrição
Feasibility 3D Perfusion Ultrasound for Liver Cancer SABR Planning and Response Evaluation; ODM derived from: https://clinicaltrials.gov/show/NCT02424955
Link
https://clinicaltrials.gov/show/NCT02424955
Palavras-chave
Versões (1)
- 29/06/2020 29/06/2020 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
29 de junho de 2020
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Liver Cancer NCT02424955
Eligibility Liver Cancer NCT02424955
- StudyEvent: Eligibility
Similar models
Eligibility Liver Cancer NCT02424955
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Informed Consent
Item
ability to understand and willingness to sign the written informed consent document
boolean
C0021430 (UMLS CUI [1])
Malignant neoplasm of liver | Secondary malignant neoplasm of liver | Stereotactic Ablative Radiotherapy Scheduled
Item
patient with primary liver tumor or metastasis scheduled for stereotactic ablative radiotherapy (sabr)
boolean
C0345904 (UMLS CUI [1])
C0494165 (UMLS CUI [2])
C4763970 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
C0494165 (UMLS CUI [2])
C4763970 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Age | Racial group | Ethnic group
Item
patient is at least 18 years of age. no gender/race-ethnic restrictions.
boolean
C0001779 (UMLS CUI [1])
C0034510 (UMLS CUI [2])
C0015031 (UMLS CUI [3])
C0034510 (UMLS CUI [2])
C0015031 (UMLS CUI [3])
ECOG performance status
Item
performance status (ecog) between 0-3
boolean
C1520224 (UMLS CUI [1])
Study Subject Participation Status | Completion of clinical trial Previous
Item
patient has previously been enrolled in and completed this study.
boolean
C2348568 (UMLS CUI [1])
C2732579 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
C2732579 (UMLS CUI [2,1])
C0205156 (UMLS CUI [2,2])
Shunt right-left intracardiac | Bidirectional cardiac shunt | Cardiac shunt Transient
Item
known right to left cardiac shunt, bidirectional or transient.
boolean
C0489644 (UMLS CUI [1])
C2711453 (UMLS CUI [2])
C0232180 (UMLS CUI [3,1])
C0205374 (UMLS CUI [3,2])
C2711453 (UMLS CUI [2])
C0232180 (UMLS CUI [3,1])
C0205374 (UMLS CUI [3,2])
Medical condition Limiting Protocol Compliance | Circumstances Limiting Protocol Compliance
Item
patient has any medical condition or other circumstances which would significantly decrease the chances of obtaining reliable data, achieving study objectives, or completing the study and/or post-dose follow-up examinations.
boolean
C3843040 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0680082 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
C0439801 (UMLS CUI [1,2])
C0525058 (UMLS CUI [1,3])
C0680082 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0525058 (UMLS CUI [2,3])
Contrast media allergy
Item
history of hypersensitivity to the contrast agent definity
boolean
C0570562 (UMLS CUI [1])
Pulmonary Hypertension
Item
history of pulmonary hypertension
boolean
C0020542 (UMLS CUI [1])
Pregnancy | Trying to conceive
Item
patients who are pregnant or are trying to become pregnant
boolean
C0032961 (UMLS CUI [1])
C0420843 (UMLS CUI [2])
C0420843 (UMLS CUI [2])