Viewing Study NCT00188552



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Study NCT ID: NCT00188552
Status: TERMINATED
Last Update Posted: 2010-08-13
First Post: 2005-09-12

Brief Title: The Use of Pentoxifylline and Vitamin E in the Treatment of Late Radiation Related Injuries
Sponsor: University Health Network Toronto
Organization: University Health Network Toronto

Study Overview

Official Title: A Phase II Study of the Use of Pentoxifylline and Vitamin E in the Treatment of Late Radiation Related Injuries
Status: TERMINATED
Status Verified Date: 2010-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: May 2007 No annual renewal
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Patients with radiation induced injuries experience significant pain and negative effects on quality of life Currently no standard therapy for these patients exists with some patients treated symptomatically and others treated with hyperbaric oxygen or pentoxifyllineVitamin E This study will examine prospectively the safety and efficacy of using a regimen of pentoxifylline and vitamin E in patients with late radiation induced injuries
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None