ID

41136

Beschrijving

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

Trefwoorden

Versies (1)
  1. 29-06-20 29-06-20 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

29 juni 2020

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Liver Cancer NCT02424955

Engels

Eligibility Liver Cancer NCT02424955

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
ability to understand and willingness to sign the written informed consent document
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
patient with primary liver tumor or metastasis scheduled for stereotactic ablative radiotherapy (sabr)
Beschrijving

Malignant neoplasm of liver | Secondary malignant neoplasm of liver | Stereotactic Ablative Radiotherapy Scheduled

Datatype

boolean

Alias
UMLS CUI [1]
C0345904
UMLS CUI [2]
C0494165
UMLS CUI [3,1]
C4763970
UMLS CUI [3,2]
C0205539
patient is at least 18 years of age. no gender/race-ethnic restrictions.
Beschrijving

Age | Racial group | Ethnic group

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0034510
UMLS CUI [3]
C0015031
performance status (ecog) between 0-3
Beschrijving

ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient has previously been enrolled in and completed this study.
Beschrijving

Study Subject Participation Status | Completion of clinical trial Previous

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C2732579
UMLS CUI [2,2]
C0205156
known right to left cardiac shunt, bidirectional or transient.
Beschrijving

Shunt right-left intracardiac | Bidirectional cardiac shunt | Cardiac shunt Transient

Datatype

boolean

Alias
UMLS CUI [1]
C0489644
UMLS CUI [2]
C2711453
UMLS CUI [3,1]
C0232180
UMLS CUI [3,2]
C0205374
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.
Beschrijving

Medical condition Limiting Protocol Compliance | Circumstances Limiting Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0525058
UMLS CUI [2,1]
C0680082
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0525058
history of hypersensitivity to the contrast agent definity
Beschrijving

Contrast media allergy

Datatype

boolean

Alias
UMLS CUI [1]
C0570562
history of pulmonary hypertension
Beschrijving

Pulmonary Hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0020542
patients who are pregnant or are trying to become pregnant
Beschrijving

Pregnancy | Trying to conceive

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0420843
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Similar models

Eligibility Liver Cancer NCT02424955

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
ECOG performance status
Item
performance status (ecog) between 0-3
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
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])
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])
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])
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])
Terug naar het begin van de pagina 

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