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Completed Not applicable Interventional Results available

FOLFOX Plus SIR-SPHERES MICROSPHERES Versus FOLFOX Alone in Patients With Liver Mets From Primary Colorectal Cancer

ClinicalTrials.gov ID: NCT00724503

Public ClinicalTrials.gov record NCT00724503. 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 May 5, 2026, 4:05 AM EDT

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

Official title

Randomised Comparative Study Of Folfox6m Plus Sir-Spheres® Microspheres Versus Folfox6m Alone As First Line Treatment In Patients With Nonresectable Liver Metastases From Primary Colorectal Carcinoma

Study identification

NCT ID
NCT00724503
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Sirtex Medical
Industry
Enrollment
530 participants

Conditions and interventions

Interventions

  • SIR-Spheres yttrium-90 microspheres Device
  • Systemic chemotherapy (FOLFOX) Drug

Device · Drug

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
Jul 31, 2006
Primary completion
Apr 30, 2015
Completion
Apr 30, 2015
Last update posted
Mar 25, 2019

2006 – 2015

United States locations

U.S. sites
21
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Pinnacle Oncology Hematology Scottsdale Arizona 85258
City of Hope Hospital Duarte California 91010
Florida International University College of Medicine Practice North Miami Beach Florida 33169
Vanguard Health Berwyn Illinois 60402
University of Illinois at Chicago Chicago Illinois 60612
Ingalls Memorial Hospital Harvey Illinois 80426
Adventist Hinsdale Hospital Hinsdale Illinois 60525
University of Louisville Louisville Kentucky 40202
University of Maryland Medical Center Baltimore Maryland 21201
William Beaumont Hospital Royal Oak Michigan 48073
Virginia Piper Cancer Institute Minneapolis Minnesota 55407
Holy Name Hospital Teaneck New Jersey 07666
Montefiore Medical Center The Bronx New York 10467
Carolinas Hematology-Oncology Associates Charlotte North Carolina 28203
Carolinas Medical Center Charlotte North Carolina 28203
Altru Health Systems Grand Forks North Dakota 58201
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15232
St. Mark's Hospital Salt Lake City Utah 84124
University of Washington Seattle Washington 98109
Aurora St. Luke's Medical Center Milwaukee Wisconsin 53215
Medical College of Wisconsin/Froedtert Memorial Lutheran Hospital Milwaukee Wisconsin 53226

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 90 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00724503, 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 Mar 25, 2019 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00724503 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →