A Study Comparing Oxycodone to Oxycodone/Naloxone in Moderate to Severe, Chronic Cancer Pain
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00513656|
Recruitment Status : Completed
First Posted : August 9, 2007
Last Update Posted : October 23, 2018
|Condition or disease||Intervention/treatment||Phase|
|Cancer Pain Constipation||Drug: Oxycodone Drug: Oxycodone/Naloxone||Phase 2|
This is a randomised, double-blind, active-controlled, double-dummy, parallel group study using oxycodone/naloxone and oxycodone to treat moderate to severe, chronic cancer pain. Subjects with documented history of cancer pain that requires around-the-clock opioid therapy will be included. Subjects must have a medical history of constipation that was induced by, or worsened by their opioid therapy.
After subjects have qualified for the study they will be randomised and to enter the double-blind treatment phase of the study.
Subjects will be randomised to receive either oxycodone/naloxone or oxycodone. Subjects will receive the double-blind medication for a period of 4 weeks.
Subjects who complete the double-blind phase or who discontinue due to constipation and still comply with all relevant screening inclusion and exclusion criteria will have the option to enter the 24 week extension phase. Subjects will receive open-label oxycodone/naloxone for up to 24 weeks.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||230 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||A Randomised, Double-blind, Active-controlled, Double-dummy, Parallel Group Study to Determine the Safety and Efficacy of Oxycodone/Naloxone Prolonged Release Tablets in Subjects With Moderate to Severe, Chronic Cancer Pain|
|Study Start Date :||September 2007|
|Actual Primary Completion Date :||March 2010|
|Actual Study Completion Date :||June 2010|
|Active Comparator: Oxycodone Hydrochloride Tablets||
|Experimental: Oxycodone Naloxone Tablets||
- Efficacy variable: Bowel Function Index (BFI) score. Amount of laxative medication use recorded at each assessment visit [ Time Frame: 4 weeks and a 6 month open label ]
- Efficacy variable: Brief Pain Inventory Short-Form (BPI-SF) (Cleeland, 1991). Amount of analgesic rescue medication used [ Time Frame: 4 weeks and a 6 month open label ]
- Number of bowel movements
- Modified Subjective Opiate Withdrawal Scale (SOWS)
- EuroQol EQ-5D
- EORTC QLQ-C30
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00513656
|Dr S Ahmedzai|
|Sheffield, United Kingdom|
|Principal Investigator:||Sam Ahmedzai||University of Sheffield|