Skip to content

cfDNA Methylation for Liver Cancer Recurrence Detection

Clinical Study on the Combined Detection of Plasma GNB4 and Riplet Gene Methylation for Monitoring Primary Liver Cancer Recurrence

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07466602
Enrollment
500
Registered
2026-03-12
Start date
2025-09-02
Completion date
2027-12-31
Last updated
2026-03-23

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

Conditions

Primary Liver Cancer

Brief 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.

Interventions

DIAGNOSTIC_TESTplasma GNB4 and Riplet genes methylation detection

Liver cancer patients undergo methylation testing at different follow-up time points after treatment

Sponsors

Wuhan Ammunition Life-tech Co., Ltd
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frame
sensitivityThrough study completion, an average of 1 year
specificityThrough study completion, an average of 1 year

Countries

China

Contacts

CONTACTTingting Li, phD
litingting@amswh.com+86 13317163570

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026