ID

36071

Beschreibung

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

Stichworte

Versionen (1)
  1. 13.04.19 13.04.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

13. April 2019

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT02460835

Englisch

Eligibility Hepatocellular Carcinoma NCT02460835

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must have hepatocellular carcinoma.
Beschreibung

Liver carcinoma

Datentyp

boolean

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

Tumor Extrahepatic Absent

Datentyp

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
Beschreibung

Patients Ineligible Hepatectomy Curative | Hepatectomy Refused

Datentyp

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.
Beschreibung

Effects of Prior Therapy Liver | Patient recovered

Datentyp

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).
Beschreibung

Zubrod Performance Status

Datentyp

boolean

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

Age

Datentyp

boolean

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

Organ function

Datentyp

boolean

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

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

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

Hypersensitivity Iodinated contrast agent Intravenous

Datentyp

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.
Beschreibung

Medical contraindication MRI with contrast

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0202671
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Hepatocellular Carcinoma NCT02460835

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
Zum Seitenanfang zurückkehren 

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