Hepatocellular Carcinoma Clinical Trial
Official title:
Cytidine-phosphate-guanosine (CpG) DNA in Hepatocellular Carcinoma Combination Therapy
to observe the outcome of hepatocellular carcinoma patients under the combination treatment of transcatheter arterial chemoembolization (TACE) and CpG DNA
| Status | Not yet recruiting |
| Enrollment | 100 |
| Est. completion date | October 2022 |
| Est. primary completion date | October 2022 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 55 Years to 75 Years |
| Eligibility |
Inclusion Criteria: - TNM (tumor node metastasis ) staging with non distant metastasis; no other tumors Exclusion Criteria: - having received previous treatment for liver cancer |
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Dalian University |
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | survival time | 5 years | ||
| Primary | metastasis free survival time | 5 years |
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