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Clinical Research on Circulating Tumor Cells in Monitoring the Effect and Early Recurrence of Liver Surgery for Hepatocellular Carcinom

Clinical Research on Circulating Tumor Cells in Monitoring the Effect and Early Recurrence of Liver Surgery for Hepatocellular Carcinom

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-DDD-15007405
Enrollment
Unknown
Registered
2015-10-24
Start date
2014-11-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carcinomas, Hepatocellular

Interventions

Gold Standard:
Index test:

Sponsors

Renji Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Benign liver disease Group: 1. Patients with chronic hepatitis or hepatic cirrhosis; 2. No history of HCC at an early age; 3. Confirmed diagnosis of HBV, HCV or non-virus hepatitis(alcoholic liver disease or non-alcoholic liver disease), regardless of whether receiving treatment or severty of the diease; 4. Receive no treatment relating to blood products up to 3 months before blood sampling(such as blood transplantation or Interleukin treatment). Hepatocellular Carcinoma Group: 1. Confirmed HCC diagnosis, regardless of the cause (HBV, HCV, alcoholic or non-Alcoholic). Make a definitive diagnosis of HCC by biopsy up to seven days before blood sampling If possible; 2. No history of HCC at an early age; 3. Receive no treatment for HCC before blood sampling,including operation, transplantation, radiotherapy, chemotherapy, etc.

Exclusion criteria

Exclusion criteria: For all patients 1. Minor patients (under 18 years of age); 2. Pregnant women; 3. Patients with actions limited by judiciary; 4. HCC patients received biopsy in 7 days before blood sampling; 5. Receive treatment relating to blood products in 3 months before blood sampling (such as blood transplantation or Interleukin treatment).

Design outcomes

Secondary

MeasureTime frame
AFP;overall survival;ALT;AST;HBV markers;HCV markers;

Primary

MeasureTime frame
circulating tumor cells;recurrence rate;

Countries

China

Contacts

Public ContactXIA QIANG
xiaqiang@shsmu.edu.cn+86 21 68383775

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026