Age
Item
1. male or female, age ≥ 20 years old.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
2. patient who accepts to enter the study by signing written informed consent.
boolean
C0021430 (UMLS CUI [1])
ECOG performance status
Item
3. patient with performance status ≤ 2 eastern cooperative oncology group (ecog).
boolean
C1520224 (UMLS CUI [1])
Liver Cirrhosis | Chronic liver disease | Nodule of liver Diameter Quantity | Nodule of liver Diameter Ultrasonography | Nodule of liver Diameter Computed Tomography | Nodule of liver Diameter MRI | Patient Therapy naive | Liver carcinoma Suspicious | Benign Neoplasm | Hemangioma | Adenoma | Focal Nodular Hyperplasia | Metastatic Lesion Cancer Other
Item
4. patient with cirrhosis or chronic liver diseases suspected to have at least 1 hepatic nodule larger than 1 cm in diameter detected by conventional image (us, ct, mri). patient who has not yet received any therapy relevant to the aforementioned diagnosis. hepatic nodule is defined as any one of the following conditions: suspicious hepatocellular carcinoma, benign tumor such as hemangioma, adenoma or focal nodular hyperplasia, metastatic lesions from other primary malignancy.
boolean
C0023890 (UMLS CUI [1])
C0341439 (UMLS CUI [2])
C0745761 (UMLS CUI [3,1])
C1301886 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C0745761 (UMLS CUI [4,1])
C1301886 (UMLS CUI [4,2])
C0041618 (UMLS CUI [4,3])
C0745761 (UMLS CUI [5,1])
C1301886 (UMLS CUI [5,2])
C0040405 (UMLS CUI [5,3])
C0745761 (UMLS CUI [6,1])
C1301886 (UMLS CUI [6,2])
C0024485 (UMLS CUI [6,3])
C0030705 (UMLS CUI [7,1])
C0919936 (UMLS CUI [7,2])
C2239176 (UMLS CUI [8,1])
C0750493 (UMLS CUI [8,2])
C0086692 (UMLS CUI [9])
C0018916 (UMLS CUI [10])
C0001430 (UMLS CUI [11])
C0333980 (UMLS CUI [12])
C1513183 (UMLS CUI [13,1])
C1707251 (UMLS CUI [13,2])
Gender Contraceptive methods
Item
5. female patient must take reliable contraception method(s) during the participation of the study.
boolean
C0079399 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Hypersensitivity 18F-FDG | Hypersensitivity 18F-FCH
Item
1. patient has serious allergic history or known allergy to 18f-fdg or 18f-fch.
boolean
C0020517 (UMLS CUI [1,1])
C0046056 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C1872806 (UMLS CUI [2,2])
Multiple malignancy
Item
2. patient has been diagnosed of multiple malignancies.
boolean
C0346429 (UMLS CUI [1])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
3. female patient who is pregnant, lactating or planning to become pregnant during the study.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Study Subject Participation Status | Research study
Item
4. patient has been participated in other investigational trials within 28 days prior to study enrollment.
boolean
C2348568 (UMLS CUI [1])
C0681814 (UMLS CUI [2])
PET/CT scan Unable
Item
5. patient is unable to undergo pet/ct scan.
boolean
C1699633 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Sepsis | Medical condition Affecting Action Radiotracer | Medical condition Affecting Uptake Radiotracer | Medical condition Affecting Elimination Radiotracer
Item
6. subjects with active systemic infections, or medical conditions that may significantly affect action, adequate uptake and elimination of radiotracer.
boolean
C0243026 (UMLS CUI [1])
C3843040 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C3266814 (UMLS CUI [2,3])
C0597354 (UMLS CUI [2,4])
C3843040 (UMLS CUI [3,1])
C0392760 (UMLS CUI [3,2])
C0243144 (UMLS CUI [3,3])
C0597354 (UMLS CUI [3,4])
C3843040 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C0221102 (UMLS CUI [4,3])
C0597354 (UMLS CUI [4,4])
Condition Study Subject Participation Status Inappropriate
Item
7. subject with conditions judged by the investigator as unsuitable for the study.
boolean
C0348080 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])