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Bioinformation Therapy for Liver Cancer

Combination of Cancer Ablation and Life Information Rehabilitation Therapy for Unresectable Liver Cancer

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03239158
Enrollment
120
Registered
2017-08-03
Start date
2017-09-02
Completion date
2018-09-02
Last updated
2019-01-25

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

Conditions

Liver, Cancer of, Non-Resectable

Keywords

Cancer ablation, Life information rehabilitation therapy

Brief summary

The aim of this study is the synergistic effect of cancer ablation and life information rehabilitation therapy on unresectable liver cancer.

Detailed description

By enrolling patients with unresectable liver cancer adapted to enrolled criteria, this study will document for the first time the synergistic effect of cancer ablation and life information rehabilitation therapy. The efficacy will be evaluated according to local relief degree, progress free survival (PFS) and overall survival (OS).

Interventions

Tumors bigger than 2 cm are fit for ablation therapy, percutaneously under CT scan or ultrasound.

Each treatment: one bottle solution each day, consecutive 3 months, oral administration

Sponsors

Shengxin Biotechnology Institute, Beijing
CollaboratorOTHER
Fuda Cancer Hospital, Guangzhou
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* All standard therapies have failed according to NCCN guidelines or the patient refuses standard therapies * Body tumor 1-6, with at least one tumor length \> 2 cm * KPS ≥ 70, lifespan \> 6 months * Platelet count ≥ 80×109/L,white blood cell count ≥ 3×109/L, neutrophil count ≥ 2×109/L, hemoglobin ≥ 80 g/L

Exclusion criteria

* Patients with cardiac pacemaker * Patients with brain metastasis * Patients with grade 3 hypertension or diabetic complication, severe cardiac and pulmonary dysfunction

Design outcomes

Primary

MeasureTime frameDescription
Relief degree of tumors3 monthsIt will be evaluated by the Response Evaluation Criteria in Solid Tumors(RECIST)

Secondary

MeasureTime frameDescription
Progress free survival(PFS)1 yearThe duration between treatment and cancer recurrence
Overall survival(OS)3 yearsThe duration between treatment and patient pass away

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026