CClinicalTrials.gg
Status unknownNCT02743065SUPER-ChinaUpdated Sep 20, 2018

HepaSphere Chemoembolization in Advanced HCC Patients: Safety & Efficacy Registry in China

An observational study in Hepatocellular Carcinoma, sponsored by Fifth Affiliated Hospital, Sun Yat-Sen University. Status unknown at 6 sites in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-09-20.

Sponsored by Fifth Affiliated Hospital, Sun Yat-Sen University · Observational

The sponsor has not verified this record recently (last verified Sep 2018), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
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Study summary

The purpose of this multicenter registry is to gather the safety, efficacy and survival data in advanced HCC patients treated with HepaSphere in China in order to evaluate the application of HepaSphere deTACE in treating advanced HCC patients

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Conditions studied

  • Hepatocellular Carcinoma

Keywords

  • HepaSphere
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In context

Carcinoma, Hepatocellular

3,182 studies on the registry are indexed under Carcinoma, Hepatocellular; 954 are open to participants now.

This study's planned enrollment of 100 is below the median of 200 across 754 observational studies indexed under Carcinoma, Hepatocellular.

Browse Carcinoma, Hepatocellular studies →

Lead sponsor

Fifth Affiliated Hospital, Sun Yat-Sen University is the lead sponsor of 57 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Subjects with Advanced Hepatocellular Carcinoma (HCC)

Inclusion criteria

  1. Age 18 or older
  2. Patient has signed informed consent
  3. Patient must have a diagnosis of hepatocellular cancer by at least one of the following method:

    1. Histological confirmation
    2. Classic imaging characteristics of HCC: Early enhancement (Arterial hypervascularity) and Venous or Delayed phase washout in multidetector contrast enhanced computed tomography (CT) scan / dynamic contrast-enhanced magnetic resonance imaging (MRI) imaging.

      • Either CT/ MRI shows at least one solid liver lesion ≥ 2 cm with the above described imaging characteristics of HCC.
      • In case of liver lesion between 1 and 2 cm, both CT and MRI imaging have to be performed in order to confirm the imaging characteristics of HCC.
  4. At time of study entry.

    1. Patients not suitable for ablation due to lesion location may be enrolled
    2. Patients with HCC recurrence but not suitable for resection or ablation maybe enrolled
  5. Patient MUST be with BCLC stage C and meet the following criteria:

    • Stage Child-Pugh A or B AND
    • Performance status ECOG ≤ 2 WITH Vascular Invasion or WITHOUT Vascular invasion
  6. Patient has a life expectancy of at least 6 months

Exclusion criteria

Exclusion Criteria:

  1. Current or previous treatment with chemo- or radiation therapy or sorafenib
  2. Previous treatment of transarterial chemoembolization (TACE)
  3. Patients with current or history of any other cancer except non-melanomatous skin cancer
  4. Female patients who are pregnant, breastfeeding, or premenopausal and not using an effective method of contraceptive
  5. Performance status ECOG > 2
  6. Child-Pugh Class C
  7. Occlusive tumor thrombus to the main portal trunk
  8. Active gastrointestinal bleeding
  9. Evidence of uncorrectable bleeding diathesis
  10. Extra-Hepatic spread of the HCC
  11. >50% tumor involvement of the liver
  12. Infiltrative HCC
  13. Encephalopathy not adequately controlled medically
  14. Presence of ascites not controlled medically
  15. Any contraindication for MRI/ CT (eg. metallic implants)
  16. Allergy to contrast media that cannot be managed with prophylaxis
  17. Any contraindication to arteriography
  18. Any contraindication for doxorubicin administration
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Device: HepaSphere Microspheres

    HepaSphere Microsphere

    Device: HepaSphere with 50-75mg Doxorubicin

Interventions

  • DeviceHepaSphere with 50-75mg Doxorubicin

    HepaSphere with 50-75mg Doxorubicin

    Also known as: Superaborbent Polymer Microsphere

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What researchers measure

Primary outcomes

  1. Adverse Events

    Time frame: 2- years

  2. Progress-free-survival (PFS)

    Time frame: 2-years

Secondary outcomes

  1. Overall Survival

    Time frame: 2-years

  2. Objective Response Rates

    Time frame: 6-months

07

Study locations

4 of 6 sites recruiting
  • Cancer Hospital Chinese Academy of Medical Science
    Beijing, China
    Active, not recruiting
  • Peking Union Medical College Hospital
    Beijing, China
    • Ning Yang, MD · Contact
    Recruiting
  • Fifth Affiliated Hospiatl, Sun Yet-Sen University
    Guangzhou, China
    • Hong Shan, MD · Contact
    • Long Fei Peng, MD · Contact
    Recruiting
  • Nanfang Hospital, Southern Medical University
    Guangzhou, China
    • Xiaofeng He, MD · Contact
    Recruiting
  • Third Affiliated Hospiatl, Sun Yet-Sen Hospital
    Guangzhou, China
    • Mingsheng Huang, MD · Contact
    • Junwei Chen, MD · Contact · aaronchan83@163.com · +86 020 85252066
    Recruiting
  • Zhongshan Hospital, Fudan University
    Shanghai, China
    Active, not recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 20, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02743065
Lead sponsor
Fifth Affiliated Hospital, Sun Yat-Sen University
Collaborators
Third Affiliated Hospital, Sun Yat-Sen University
Responsible party
Hong Shan (Professor, Fifth Affiliated Hospital, Sun Yat-Sen University) — Principal investigator
First posted
Apr 19, 2016
Start date
Sep 2016
Primary completion
Jun 2019 (estimated)
Completion
Dec 2019 (estimated)
Last update
Sep 20, 2018

Study contacts

Mingsheng Huang, MD
Contact
+86 020 85252066
Junwei Chen
Contact
aaronchan83@163.com
+86 020 85252066
Hong Shan, MD
principal investigator · Fifth Affiliated Hospiatl, Sun Yet-Sen University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2018. You cannot join it, but the record below documents what was studied.

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