Clinical Trials Directory

Trials / Completed

CompletedNCT00183911

Study of 5-Fluorouracil and Leucovorin and Intra-abdominal Floxuridine Chemoradiation in Patients With Fully Resected Locally Advanced Gastric Adenocarcinoma

Phase II Study of Adjuvant Intraperitoneal FUDR Treatment Added to Chemoradiation (5-Fluorouracil/Leucovorin Plus Total Dose 4500 cGy of External Beam Radiotherapy) in Patients With Fully Resected Locally Advanced Gastric Adenocarcinoma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
25 (estimated)
Sponsor
University of Southern California · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the side effects of a new treatment for stomach cancer which may potentially improve the prognosis of this cancer. Our principle objective is to improve the results of standard chemotherapy and radiation after surgery of patients with gastric cancer. The intra-abdominal (intraperitoneal) administration of floxuridine (FUDR) is a procedure that we have studied and have determined it is a safe treatment. In this study, we want to evaluate the side effects of this treatment when it is given after surgery but before standard intravenous chemotherapy and radiation. Study treatment will start with surgical removal of the part of the stomach with cancer, together with surrounding tissues and lymph nodes. After surgery, patients will get treatment with a chemotherapy drug, FUDR, administered directly into the abdomen. This is called intraperitoneal chemotherapy. After this treatment patients will receive repeated intravenous injection of two drugs, 5-fluorouracil and leucovorin alone or combined with irradiation of the abdomen.

Conditions

Interventions

TypeNameDescription
DRUGfloxuridine, 5-Fluorouracil, leucovorin
PROCEDUREExternal Beam Radiotherapy
PROCEDURESurgery

Timeline

Start date
2003-11-01
Primary completion
2006-12-01
Completion
2007-04-01
First posted
2005-09-16
Last updated
2014-05-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00183911. Inclusion in this directory is not an endorsement.