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Spots Global Cancer Trial Database for Amifostine in Treating Peripheral Neuropathy in Patients Who Have Received Chemotherapy for Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Amifostine in Treating Peripheral Neuropathy in Patients Who Have Received Chemotherapy for Cancer

Official Title: A Randomized Phase III Trial of Amifostine vs. No Treatment for Platinum Induced Peripheral Neuropathy

Study ID: NCT00058071

Study Description

Brief Summary: RATIONALE: Amifostine may be effective in relieving numbness, tingling, and other symptoms of peripheral neuropathy. It is not yet known whether amifostine is effective in treating peripheral neuropathy in patients who have received chemotherapy for cancer. PURPOSE: This randomized phase III trial is studying amifostine to see how well it works compared to observation in relieving numbness, tingling, and other symptoms of peripheral neuropathy in patients who have received platinum-based chemotherapy (such as cisplatin or carboplatin) for cancer.

Detailed Description: OBJECTIVES: * Determine, preliminarily, whether amifostine is superior to no treatment, in terms of improving the symptoms and/or objective findings of platinum-induced peripheral neuropathy, in patients with cancer. * Determine the toxicity of this drug in these patients. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive amifostine IV or subcutaneously over 3 minutes on days 1, 3, and 5. Treatment continues for 12 weeks in the absence of unacceptable toxicity. Patients are observed for 12 weeks. * Arm II: Patients are observed for 24 weeks. After 24 weeks patients may cross over to treatment as in arm I. Quality of life is assessed at baseline and then at 6, 12, 18, and 24 weeks after study entry. Patients are followed at 6 and 12 weeks after study treatment, every 3 months for 2 years, every 6 months for 3 years, and then annually thereafter. PROJECTED ACCRUAL: A total of 50-100 patients (25-50 per treatment arm) will be accrued for this study.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Providence Saint Joseph Medical Center - Burbank, Burbank, California, United States

Moores UCSD Cancer Center, La Jolla, California, United States

Jonsson Comprehensive Cancer Center at UCLA, Los Angeles, California, United States

George Bray Cancer Center at the Hospital of Central Connecticut - New Britain Campus, New Britain, Connecticut, United States

St. Vincent's Medical Center, Jacksonville, Florida, United States

Ella Milbank Foshay Cancer Center at Jupiter Medical Center, Jupiter, Florida, United States

Lakeland Regional Cancer Center at Lakeland Regional Medical Center, Lakeland, Florida, United States

University of Miami Sylvester Comprehensive Cancer Center - Miami, Miami, Florida, United States

Curtis & Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center, Savannah, Georgia, United States

Rush-Copley Cancer Care Center, Aurora, Illinois, United States

Robert H. Lurie Comprehensive Cancer Center at Northwestern University, Chicago, Illinois, United States

University of Illinois Cancer Center, Chicago, Illinois, United States

Ingalls Cancer Care Center at Ingalls Memorial Hospital, Harvey, Illinois, United States

Hinsdale Hematology Oncology Associates, Hinsdale, Illinois, United States

Joliet Oncology-Hematology Associates, Limited - West, Joliet, Illinois, United States

Regional Cancer Center at Memorial Medical Center, Springfield, Illinois, United States

Carle Cancer Center at Carle Foundation Hospital, Urbana, Illinois, United States

CCOP - Carle Cancer Center, Urbana, Illinois, United States

Elkhart General Hospital, Elkhart, Indiana, United States

Howard Community Hospital at Howard Regional Health System, Kokomo, Indiana, United States

Center for Cancer Therapy at LaPorte Hospital and Health Services, La Porte, Indiana, United States

Saint Anthony Memorial Health Centers, Michigan City, Indiana, United States

CCOP - Northern Indiana CR Consortium, South Bend, Indiana, United States

Memorial Hospital of South Bend, South Bend, Indiana, United States

Saint Joseph Regional Medical Center, South Bend, Indiana, United States

Holden Comprehensive Cancer Center at University of Iowa, Iowa City, Iowa, United States

Louisville Oncology at Norton Cancer Center, Louisville, Kentucky, United States

William Beaumont Hospital - Royal Oak Campus, Royal Oak, Michigan, United States

Lakeland Regional Cancer Care Center - St. Joseph, St. Joseph, Michigan, United States

University of Mississippi Cancer Clinic, Jackson, Mississippi, United States

CCOP - Cancer Research for the Ozarks, Springfield, Missouri, United States

St. John's Regional Health Center, Springfield, Missouri, United States

Hulston Cancer Center at Cox Medical Center South, Springfield, Missouri, United States

Siteman Cancer Center at Barnes-Jewish Hospital, St Louis, Missouri, United States

Women's Cancer Center - Lake Mead, Las Vegas, Nevada, United States

Sunrise Hospital and Medical Center, Las Vegas, Nevada, United States

Fox Chase Virtua Health Cancer Program at Virtua Memorial Hospital Marlton, Marlton, New Jersey, United States

Cancer Institute of New Jersey at Cooper - Voorhees, Voorhees, New Jersey, United States

Fox Chase Virtua Health Cancer Program at Virtua West Jersey, Voorhees, New Jersey, United States

SUNY Downstate Medical Center, Brooklyn, New York, United States

Roswell Park Cancer Institute, Buffalo, New York, United States

Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill, Chapel Hill, North Carolina, United States

Blumenthal Cancer Center at Carolinas Medical Center, Charlotte, North Carolina, United States

FirstHealth Moore Regional Community Hospital Comprehensive Cancer Center, Pinehurst, North Carolina, United States

McDowell Cancer Center at Akron General Medical Center, Akron, Ohio, United States

Aultman Hospital Cancer Center at Aultman Health Foundation, Canton, Ohio, United States

Charles M. Barrett Cancer Center at University Hospital, Cincinnati, Ohio, United States

Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University, Columbus, Ohio, United States

Riverside Methodist Hospital Cancer Care, Columbus, Ohio, United States

Mount Carmel Health - West Hospital, Columbus, Ohio, United States

Hillcrest Cancer Center at Hillcrest Hospital, Mayfield Heights, Ohio, United States

Oklahoma University Cancer Institute, Oklahoma City, Oklahoma, United States

Cancer Care Associates - Midtown Tulsa, Tulsa, Oklahoma, United States

Rosenfeld Cancer Center at Abington Memorial Hospital, Abington, Pennsylvania, United States

Fox Chase Cancer Center - Philadelphia, Philadelphia, Pennsylvania, United States

Avera Cancer Institute, Sioux Falls, South Dakota, United States

Sioux Valley Hospital and University of South Dakota Medical Center, Sioux Falls, South Dakota, United States

Contact Details

Name: Steven C. Plaxe, MD

Affiliation: University of California, San Diego

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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