Trials / Completed
CompletedNCT01031784
Radioactive Holmium Microspheres for the Treatment of Liver Metastases
Radioactive Holmium Microspheres for the Treatment of Patients With Non-resectable Liver Metastases of Mixed Origin; a Single Center, Interventional, Non-randomized, Open Label, Safety Study.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 15 (actual)
- Sponsor
- UMC Utrecht · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The HEPAR study is aimed at determining the safety of radioactive holmium containing microspheres for the treatment of tumors in the liver. These microspheres will be administered by infusion in the liver artery using a arterial catheter in the femoral artery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | holmium-166 poly lactic acid microspheres | Intra arterial administration of radioactive Holmium 166 microspheres; 600 mg with a specific activity ranging from 1260 MBq per kilo liver weight to 5040 MBq in the highest dose |
| DEVICE | holmium 166 microspheres | intra arterial administration of holmium 166 microsphers in the hepatic artery |
Timeline
- Start date
- 2009-12-01
- Primary completion
- 2011-12-01
- Completion
- 2011-12-01
- First posted
- 2009-12-15
- Last updated
- 2012-01-31
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT01031784. Inclusion in this directory is not an endorsement.