CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 261 enrolled
Drug / intervention
Oxycodone/naloxonedrug
Likely dose
Not stated in 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/NCT01811186
NCT01811186Phase 4Completed

An Interventional Study to Compare the Efficacy and Tolerability of Current and Slow Titration With Targin® in the Treatment of Moderate to Severe Non-malignant Chronic Pain (GLORY)

Mundipharma Korea Ltd·interventional·Posted Mar 14, 2013·Updated Mar 10, 2017

In Brief

A Phase 4 clinical trial evaluating Oxycodone/naloxone for Chronic Pain. Completed, enrolled 261 participants across 1 site.

Detailed Summary

Objectives: 1. Objective of main interest \- To assess the drop-out rate caused by adverse event\* after 6 weeks treatment 2. Further objectives * To assess the drop-out rate caused by adverse event\* after 1 week treatment * To assess the pain reduction rate after 6 weeks treatment from baseline * To assess the Euroquol (EQ-5D) quality of life * To assess physician's overall satisfaction * To assess subject's overall satisfaction * To assess safety

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsChronic Pain
CountriesSouth Korea
Collaborators--

Timeline

Phase 4CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMar 14, 2013
Enrollment StartDec 1, 2012
Primary CompletionJan 1, 2014
Study CompletionJun 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 13.3 years ago

Interventions

Oxycodone/naloxonedrug

Oxycodone/naloxone titration