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Recruiting Observational

cfDNA Methylation for Liver Cancer Recurrence Detection

NCT07466602 · tracked via the Priya Life Science China tracker
Sponsor
Wuhan Ammunition Life-tech Co., Ltd
Phase
Observational
Started
2025-09-02
Last updated
2026-03-23

Condition(s) studied

Primary Liver Cancer

Investigational drug(s) / intervention(s)

plasma GNB4 and Riplet genes methylation detection

plasma GNB4 and Riplet genes methylation detection: Liver cancer patients undergo methylation testing at different follow-up time points after treatment

Study summary

Through follow-up testing of patients with primary liver cancer who underwent hepatectomy, liver transplantation, ablation therapy, or transarterial chemoembolization (TACE), a blinded comparative trial was conducted at each monitoring site. This trial evaluated the combined methylation detection kit for GNB4 and Riplet genes (fluorescent PCR method) against the clinical reference standard (defined as the physician's comprehensive diagnosis based on clinical guidelines and other criteria). The study evaluated the clinical performance of the assay in diagnosing primary liver cancer recurrence and validated the clinical efficacy of methylation detection kits for monitoring recurrence after primary liver cancer treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Primary liver cancer Exclusion Criteria: * Concurrent other malignant tumors; * Ineligible for hepatectomy, liver transplantation, ablation, or TACE therapy; * Negative methylation status prior to treatment.

Primary outcome measure(s)

  • sensitivity — Through study completion, an average of 1 year
  • specificity — Through study completion, an average of 1 year

Trial sites (1)

FacilityCityRegionStatus
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07466602 on ClinicalTrials.gov ↗ ← All trials in China