Clinical Efficacy of Transarterial Infusion Chemotherapy for Unresectable Colorectal Cancer

NCT07333053 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-03-06

No results posted yet for this study

Summary

This is a prospective, multicenter, randomized, and open-label clinical trial. It is initiated to determine the efficacy of FOLFOX-based, transarterial infusion chemotherapy (TAIC) combined with either cetuximab or bevacizumab for patients with unresectable colorectal cancer (CRC).

Conditions

  • Unresectable Colorectal Cancer

Interventions

PROCEDURE

Transarterial infusion chemotherapy (TAIC)

TAIC can increase the local intra-tumoral concentrations of chemotherapeutic agents by intensifying drug delivery into the tumor via super-selective catheterization of the tumor-feeding artery, and meanwhile reduce systematic toxicity.

PROCEDURE

Intravenous Chemotherapy(IVC)

Intravenous administration of chemotherapeutic agents is the mainstay of chemotherapy.

Sponsors & Collaborators

  • Liaoning Cancer Hospital & Institute

    collaborator OTHER
  • The Rocket Force Characteristic Medical Center

    collaborator UNKNOWN
  • Second Affiliated Hospital of Nanchang University

    collaborator OTHER
  • The Affiliated Hospital of Hebei University

    collaborator UNKNOWN
  • The First Hospital of Qinhuangdao

    collaborator OTHER_GOV
  • The Central Hospital of Handan City

    collaborator UNKNOWN
  • The First People's Hospital of Jiujiang City

    collaborator UNKNOWN
  • Changzhi Medical College

    collaborator OTHER
  • Zibo Boshan District Traditional Chinese Medicine Hospital

    collaborator UNKNOWN
  • Linshu County People's Hospital

    collaborator UNKNOWN
  • Hebei Yixian Hospital

    collaborator UNKNOWN
  • Baoding Mancheng District People's Hospital

    collaborator UNKNOWN
  • Quanda Liu

    lead OTHER

Principal Investigators

  • Quanda Liu, MD · Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-31
Primary Completion
2027-12-31
Completion
2027-12-31

Countries

  • China

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07333053 on ClinicalTrials.gov