CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 30 enrolled
Drug / intervention
Oxycodone +1 moredrug
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/NCT03176199
NCT03176199Phase 4Completed

An Interventional, Open Label, and Randomized Controlled Study to Compare the Titration Efficacy and Safety of Control-released Oxycodone and Immediate-released Oxycodone in Opioid-naive Patients With Moderate to Severe Cancer Pain

Taiwan Mundipharma Pharmaceuticals Ltd.·interventional·Posted Jun 5, 2017·Updated Mar 18, 2020

In Brief

A Phase 4 clinical trial evaluating Oxycodone for Cancer and Pain. Completed, enrolled 30 participants across 4 sites.

Detailed Summary

This study is to evaluate the efficacy and safety of a titration method by selects 10 mg control-released (CR) oxycodone tablet as background drug in combined with immediate-released (IR) oxycodone, compared to conventional titration method with immediate-released (IR) oxycodone in patients with moderate to severe cancer pain in Taiwan.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsCancer, Pain
CountriesTaiwan
Collaborators--

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedJun 5, 2017
Enrollment StartSep 1, 2016
Primary CompletionDec 31, 2018
TodayJul 2, 2026
Enrollment to primary: 2.3 yearsPosted 9.1 years ago

Interventions

Oxycodonedrug

Every 12 hours for control-released oxycodone (OxyContin®)

Oxycodonedrug

Every 6 hours for immediate-released oxycodone (OxyNorm®)