ID

36071

Description

A Pilot Study of Individualized Adaptive Radiation Therapy for Hepatocellular Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02460835

Link

https://clinicaltrials.gov/show/NCT02460835

Keywords

Versions (1)
  1. 4/13/19 4/13/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

April 13, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT02460835

English

Eligibility Hepatocellular Carcinoma NCT02460835

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must have hepatocellular carcinoma.
Description

Liver carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C2239176
patients must not have extrahepatic cancer.
Description

Tumor Extrahepatic Absent

Data type

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C1517058
UMLS CUI [1,3]
C0332197
patients must not be eligible for a curative liver resection or have refused resection
Description

Patients Ineligible Hepatectomy Curative | Hepatectomy Refused

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1512714
UMLS CUI [1,3]
C0019144
UMLS CUI [1,4]
C1276305
UMLS CUI [2,1]
C0019144
UMLS CUI [2,2]
C1705116
patients must have recovered from the acute effects of prior liver-directed therapy and 4 weeks must have passed since the last procedure and protocol therapy.
Description

Effects of Prior Therapy Liver | Patient recovered

Data type

boolean

Alias
UMLS CUI [1,1]
C1704420
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0023884
UMLS CUI [2]
C1115804
patients must have a zubrod performance status of less than or equal to 2 (zubrod performance status is a measure that attempts to quantify a cancer patients' general well-being. scores run from 0 to 5 where 0 denotes normal activity and 5 denotes death).
Description

Zubrod Performance Status

Data type

boolean

Alias
UMLS CUI [1]
C3714786
patients must be 18 years of age or older.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patients must have adequate organ function.
Description

Organ function

Data type

boolean

Alias
UMLS CUI [1]
C0678852
patients must understand and be willing to sign an irb (institutional review board) approved informed consent form.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with known allergies to intravenous iodinated contrast agents.
Description

Hypersensitivity Iodinated contrast agent Intravenous

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0879373
UMLS CUI [1,3]
C1522726
patients with a contraindication to contrast-enhanced mri are excluded.
Description

Medical contraindication MRI with contrast

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0202671
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Similar models

Eligibility Hepatocellular Carcinoma NCT02460835

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Liver carcinoma
Item
patients must have hepatocellular carcinoma.
boolean
C2239176 (UMLS CUI [1])
Tumor Extrahepatic Absent
Item
patients must not have extrahepatic cancer.
boolean
C0027651 (UMLS CUI [1,1])
C1517058 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Patients Ineligible Hepatectomy Curative | Hepatectomy Refused
Item
patients must not be eligible for a curative liver resection or have refused resection
boolean
C0030705 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
C0019144 (UMLS CUI [1,3])
C1276305 (UMLS CUI [1,4])
C0019144 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Effects of Prior Therapy Liver | Patient recovered
Item
patients must have recovered from the acute effects of prior liver-directed therapy and 4 weeks must have passed since the last procedure and protocol therapy.
boolean
C1704420 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0023884 (UMLS CUI [1,3])
C1115804 (UMLS CUI [2])
Zubrod Performance Status
Item
patients must have a zubrod performance status of less than or equal to 2 (zubrod performance status is a measure that attempts to quantify a cancer patients' general well-being. scores run from 0 to 5 where 0 denotes normal activity and 5 denotes death).
boolean
C3714786 (UMLS CUI [1])
Age
Item
patients must be 18 years of age or older.
boolean
C0001779 (UMLS CUI [1])
Organ function
Item
patients must have adequate organ function.
boolean
C0678852 (UMLS CUI [1])
Informed Consent
Item
patients must understand and be willing to sign an irb (institutional review board) approved informed consent form.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypersensitivity Iodinated contrast agent Intravenous
Item
patients with known allergies to intravenous iodinated contrast agents.
boolean
C0020517 (UMLS CUI [1,1])
C0879373 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,3])
Medical contraindication MRI with contrast
Item
patients with a contraindication to contrast-enhanced mri are excluded.
boolean
C1301624 (UMLS CUI [1,1])
C0202671 (UMLS CUI [1,2])
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