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A prospective, randomized controlled clinical study of relation between ctDNA and recurrence and metastasis of liver cancer patients

A prospective, randomized controlled clinical study of relation between ctDNA and recurrence and metastasis of liver cancer patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROR-17012157
Enrollment
Unknown
Registered
2017-07-27
Start date
2017-08-30
Completion date
Unknown
Last updated
2017-08-21

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

Conditions

hepatic carcinoma

Interventions

1: block the vena cava before touching liver in the tumor side
2:Not block the vena cava before touching liver in the tumor side

Sponsors

Tianjin First Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: The subject will be included,who must meet all the following criteria: 1. Patients must confirmed hepatic carcinoma which TNM stage was II/III; 2. Aged 18 to 75 years; 3. Patient must provide the blood sample, and the amount should be able to meet the requirements of DNA extraction and quality control; 4. The heart, lung, kidney and other major organs of the patients meet the requirements of this study; 5. Patients must have the ability to understand and the willingness to sign a written informed consent document, willing to cooperate with the follow-up.

Exclusion criteria

Exclusion criteria: Either of the following which is not one of exclusion criteria will not be enrolled: 1. Other malignancies in the past five years;except cured basal cell carcinoma, cervical carcinoma in situ, localized prostate cancer with surgical treatment or breast ductal carcinoma in situ with surgical resection; 2. Patients with extrahepatic distal metastases; 3. Patients with infection; 4. Cognitive ability and psychological abnormality; 5. Other serious diseases that researchers believe the subject can not be enrolled; 6. Use other test drugs or participate in other clinical trials; 7. Preoperative acceptance anti-tumor therapy, such as intubation chemotherapy, anhydrous alcohol injection, radiofrequency ablation team and others.

Design outcomes

Primary

MeasureTime frame
The time between ctDNA detection and clinical relapse;cfDNA concentration;tumor mutation load;the level of AFP;OS;Recurrence rate;relapse free survival;genetic mutation;

Countries

China

Contacts

Public ContactJiangwen Tao

Tianjin First Central Hospital

Jiang-wentao@medmail.com.cn+86 13821264987

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026