CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 154 enrolled
Drug / intervention
Edaravone +1 moredrug
Likely dose
Edaravone 30mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01865201
NCT01865201Phase 2Completed

Effect of Edaravone on Radiation-induced Temporal Lobe Necrosis in Patients With Nasopharyngeal Carcinoma After Radiotherapy

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University·interventional·Posted May 30, 2013·Updated Dec 12, 2013

In Brief

A Phase 2 clinical trial evaluating Edaravone and Common fundamental management for Nasopharyngeal Carcinoma and Brain Necrosis. Completed, enrolled 154 participants across 1 site.

Detailed Summary

It is hypothesized that excessive generation of free radicals involves in the pathogenesis of radiation-induced brain necrosis. This study therefore evaluated the effect of free radical scavenger, edaravone, on radiation-induced temporal lobe necrosis (TLN) in patients with nasopharyngeal carcinoma (NPC) after radiotherapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesChina
Collaborators--

Timeline

Phase 2CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedMay 30, 2013
Enrollment StartMar 1, 2009
Primary CompletionOct 1, 2011
Study CompletionSep 1, 2012
TodayJul 1, 2026
Enrollment to primary: 2.6 yearsPosted 13.1 years ago

Interventions

Edaravonedrug

Be used at a dose of 30mg, intravenously, twice per day, for 14 days.

Common fundamental managementother

common fundamental management, which was as follows: ①Methylprednisolone, administered by intravenous infusion at a 500mg daily for 3 consecutive days and then gradually tailed off in 30 days with administration of oral prednisolone. ②Dehydration drugs.