Skip to content

A randomized, single blind controlled trial: transcatheter Arterial chemoembolization (TACE) of postoperative liver cancer by using three different drug.

A randomized, single blind controlled trial: transcatheter Arterial chemoembolization (TACE) of postoperative liver cancer by using three different drug.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TNC-09000363
Enrollment
Unknown
Registered
2009-04-02
Start date
2007-01-01
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

liver cancer

Interventions

Group A:Epirubicin hydrochloride 40mg, iodine 5ml
Group B:Genmzar 1000mg, iodine 5ml
Group C:hydroxycamptothecia 10mg, iodine 5ml
Group D:Epirubicin hydrochloride 40mg+Genmzar 1000mg, iodine 5ml
Group E:Epirubicin hydrochloride 40mg+hydroxycamptothecia 10mg, iodine 5ml
Group F:Genmzar 1000mg+hydroxycamptothecia 10mg, iodine 5ml

Sponsors

Eastern Hepatobiliary Surgery Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. postoperative liver cancer who need prevent the recurrent; 2. both male and female; 3. diagnosed 'liver cancer'; 4. without any recurrent in liver in CT or MRI; 5. Liver function (Child grade) grading higher than B (include B); 6. not received other chemotherapy or obstruct therapy.

Exclusion criteria

Exclusion criteria: Irritability for iodine; Combined with other tumours; Complicated with unstable angina, congestive heart-failure (heart function grade VI) and uncontrolled hypertension, arrhythmia, sever infection, uncontrolled and unstable diabetes.

Design outcomes

Primary

MeasureTime frame
number and size of tumor;stable and progress of illness;

Secondary

MeasureTime frame
AFP, CA19-9;

Countries

China

Contacts

Public ContactHongyan Chen
Chengys9304@yahoo.com.cn+86 021 81875211

Outcome results

None listed

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