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A randomized controlled trial of adefovir for relapse of primary liver carcinoma and liver function impairment after surgery

A randomized controlled trial of adefovir for relapse of primary liver carcinoma and liver function impairment after surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000090
Enrollment
Unknown
Registered
2008-04-18
Start date
2007-06-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Primary liver cancer

Interventions

Group A:adefovir treatment (Glaxo Smith Kline, Adefovir Dipivoxil Tablets, 10 mg p.o. Qd)
Group B:no antiviral treatment

Sponsors

Oriental Department of Liver and Gall Surgery Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. age >= 16y; 2. primary liver cancer patients with HBeAg (+) or HBVDNA >=10^5 copies/ml (PCR method); 3. liver function before surgery: Child A; 4. Clinical stage of primary liver cancer: T1N0M0 or T2N0M0 I or II stage); 5. pathologically diagnosed chronic hepatitis after surgery; 6. pathologically diagnosed primary liver cancer after surgery.

Exclusion criteria

Exclusion criteria: 1. combined infection of HIV, HCV or HDV; 2. received interferon, thymic peptide or other antiviral activity medicines (like entecavi, lamivudine, etc.) within 24 weeks when allocation; 3. received anti-HIV nucleoside or nucleoside analogue medicine more than 12 weeks.

Design outcomes

Primary

MeasureTime frame
Relapse of cancer;Quality of life;Survival rate;

Secondary

MeasureTime frame
Serum HBVDNA level;Improvemt of AFP;HBeAg negative conversion rate;improvement of histology;Improvement of liver fuction;

Countries

China

Contacts

Public ContactGang Huang
squaror@hotmail.com+86 0 13918663457

Outcome results

None listed

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