Informações:
Falhas:
ID
36071
Descrição
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
Palavras-chave
Versões (1)
- 13/04/2019 13/04/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
13 de abril de 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Hepatocellular Carcinoma NCT02460835
Eligibility Hepatocellular Carcinoma NCT02460835
- StudyEvent: Eligibility
Similar models
Eligibility Hepatocellular Carcinoma NCT02460835
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
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])
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])
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])
C0202671 (UMLS CUI [1,2])