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Terminated Phase 3 Interventional Results available

Oxaliplatin and Capecitabine With or Without an Hepatic Arterial Infusion With Floxuridine in Treating Patients Who Are Undergoing Surgery and/or Ablation for Liver Metastases Due to Colorectal Cancer

ClinicalTrials.gov ID: NCT00268463

Public ClinicalTrials.gov record NCT00268463. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 4:30 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III Clinical Trial Comparing Oxaliplatin, Capecitabine and Hepatic Arterial Infusion of Floxuridine to Oxaliplatin and Capecitabine in Patients With Resected or Ablated Liver Metastases From Colorectal Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

RATIONALE: Drugs used in chemotherapy, such as oxaliplatin, capecitabine, and floxuridine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Hepatic arterial infusion uses a catheter to carry tumor-killing substances, such as chemotherapy, directly into the liver. Giving chemotherapy in different ways may kill more tumor cells. It is not yet known whether giving oxaliplatin and capecitabine together with an hepatic arterial infusion with floxuridine is more effective than giving oxaliplatin and capecitabine alone in treating patients who are undergoing surgery and/or ablation for liver metastases due to colorectal cancer. PURPOSE: This randomized phase III trial is studying oxaliplatin, capecitabine, and an hepatic arterial infusion with floxuridine to see how well they work compared to oxaliplatin and capecitabine in treating patients who are undergoing surgery and/or ablation for liver metastases due to colorectal cancer.

Study identification

NCT ID
NCT00268463
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
NSABP Foundation Inc
Network
Enrollment
22 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 2006 (Type not available)
Primary completion
Jun 2008 (Actual)
Completion
Jun 2008 (Actual)
Last update posted
May 15, 2013

2006 – 2008

United States locations

U.S. sites
31
U.S. states
20
U.S. cities
26
Facility City State ZIP Site status
Cancer Care Center at John Muir Health - Concord Campus Concord California 94524-4110 —
City of Hope Comprehensive Cancer Center Duarte California 91010-3000 —
Veterans Affairs Medical Center - Loma Linda (Pettis) Loma Linda California 92357 —
Kaiser Permanente Medical Center - Walnut Creek Walnut Creek California 94596 —
John Muir/Mt. Diablo Comprehensive Cancer Center Walnut Creek California 94598 —
CCOP - Christiana Care Health Services Newark Delaware 19713 —
Washington Cancer Institute at Washington Hospital Center Washington D.C. District of Columbia 20010 —
Curtis & Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center Savannah Georgia 31403-3089 —
Via Christi Cancer Center at Via Christi Regional Medical Center Wichita Kansas 67214 —
Central Baptist Hospital Lexington Kentucky 40503-9985 —
Louisville Oncology at Norton Cancer Center Louisville Kentucky 40202 —
CCOP - Ochsner New Orleans Louisiana 70121 —
Harry & Jeanette Weinberg Cancer Institute at Franklin Square Hospital Center Baltimore Maryland 21237 —
Saint Joseph Mercy Cancer Center Ann Arbor Michigan 48106-0995 —
Borgess Medical Center Kalamazoo Michigan 49001 —
West Michigan Cancer Center Kalamazoo Michigan 49007-3731 —
Bronson Methodist Hospital Kalamazoo Michigan 49007 —
Mayo Clinic Cancer Center Rochester Minnesota 55905 —
Wake Forest University Comprehensive Cancer Center Winston-Salem North Carolina 27157-1096 —
Altru Cancer Center at Altru Hospital Grand Forks North Dakota 58201 —
Natalie Warren Bryant Cancer Center at St. Francis Hospital Tulsa Oklahoma 74136 —
Legacy Good Samaritan Hospital & Medical Center Comprehensive Cancer Center Portland Oregon 97210 —
CCOP - Columbia River Oncology Program Portland Oregon 97225 —
Providence St. Vincent Medical Center Portland Oregon 97225 —
St. Luke's Cancer Network at St. Luke's Hospital Bethlehem Pennsylvania 18015 —
Geisinger Medical Center Danville Pennsylvania 17822-0001 —
UMC Southwest Cancer and Research Center Lubbock Texas 79415-3364 —
Fletcher Allen Health Care - University Health Center Campus Burlington Vermont 05401 —
Virginia Oncology Associates - Hampton Hampton Virginia 23666 —
Mary Babb Randolph Cancer Center at West Virginia University Hospitals Morgantown West Virginia 26506 —
University of Wisconsin Paul P. Carbone Comprehensive Cancer Center Madison Wisconsin 53792-6164 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00268463, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 15, 2013 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00268463 live on ClinicalTrials.gov.

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