ID

41136

Beskrivning

Feasibility 3D Perfusion Ultrasound for Liver Cancer SABR Planning and Response Evaluation; ODM derived from: https://clinicaltrials.gov/show/NCT02424955

Länk

https://clinicaltrials.gov/show/NCT02424955

Nyckelord

Versioner (1)
  1. 2020-06-29 2020-06-29 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

29 juni 2020

DOI

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Licens

Creative Commons BY 4.0
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Eligibility Liver Cancer NCT02424955

Engelsk

Eligibility Liver Cancer NCT02424955

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

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

Informed Consent

Datatyp

boolean

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

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

Datatyp

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.
Beskrivning

Age | Racial group | Ethnic group

Datatyp

boolean

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

ECOG performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beskrivning

Exclusion Criteria

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

Study Subject Participation Status | Completion of clinical trial Previous

Datatyp

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.
Beskrivning

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

Datatyp

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.
Beskrivning

Medical condition Limiting Protocol Compliance | Circumstances Limiting Protocol Compliance

Datatyp

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
Beskrivning

Contrast media allergy

Datatyp

boolean

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

Pulmonary Hypertension

Datatyp

boolean

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

Pregnancy | Trying to conceive

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0420843
Tillbaka till toppen

Similar models

Eligibility Liver Cancer NCT02424955

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

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