Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Greenville, North Carolina 27834


Purpose:

The purpose of this protocol is to provide supervised and limited access to Therasphere® treatment for patients with primary liver cancer and chemotherapy refractory liver metastasis who cannot be treated by surgical removal of the affected part of the liver. Patient response to treatment and any side effects of Therasphere® treatment will be examined.


Criteria:

Inclusion Criteria: - Confirmed diagnosis of primary or metastatic intrahepatic carcinoma - The cancer must be unresectable with limited established treatment options - ECOG Performance Status Score 0-2 - Age 19 years or older - Able to comprehend and provide written informed consent Exclusion Criteria: - Any pre-treatment laboratory findings within 15 days of treatment demonstrating: - Absolute granulocyte count ≤ 1,500/ul - Platelet count ≤ 75,000/ul - Serum creatinine > 2.0 mg/dl - Serum bilirubin ≥ 2.0 mg/dl - Any of the following contraindications to angiography and selective visceral catheterization: - History of severe allergy or intolerance to any contrast media, narcotics, sedatives, or atropine - Bleeding, diathesis, not correctable by usual forms of therapy - Severe peripheral vascular disease that would preclude catheterization - Substantial venous shunt away from the liver - Evidence of potential delivery of greater than 11 mCi (20 Gy absorbed dose) of radiation to the lungs on either 1) first Therasphere® administration; or 2) cumulative delivery of radiation to the lungs over multiple treatments - Evidence of any detectable Tc-99 MAA flow to the stomach or duodenum, application of established angiographic techniques to stop such flow - Significant extrahepatic disease representing an imminent life- threatening situation outcome - Severe liver dysfunction or pulmonary insufficiency - Active uncontrolled infection - Significant underlying medical or psychiatric illness - Pregnant women may not participate


NCT ID:

NCT00701168


Primary Contact:

Principal Investigator
Suzanne Russo, MD
East Carolina University School of Medicine


Backup Contact:

N/A


Location Contact:

Greenville, North Carolina 27834
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 20, 2018

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.