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Oxycodone/Naloxone (OXN) Combination in Moderate to Severe Non-malignant Pain

Pain Clinical Trial

Official title:
An Open Study to Observe OXN Treatment for Patients With Moderate to Severe Non-malignant Pain

Clinical Trial Summary

The main objective of the study is to observe the OXN treatment of patients with moderate to severe non-malignant pain in daily clinical practise with respect to pain relief and bowel function. Patients who have insufficient pain relief and/or unacceptable side effects with the previous analgesic treatment WHO step 1 or 2 and require around-the-clock opioid therapy can be included in the study.

Clinical Trial Description

Patients will receive OXN for 3 weeks in the first phase (core phase) and in the second phase (extension phase) they will receive OXN as is daily clinical practice until reimbursement of OXN in the Netherlands or until discontinuation on request of the patient. ;

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01167127
Study type Interventional
Source Mundipharma Pharmaceuticals B.V.
Contact
Status Completed
Phase Phase 3
Start date June 2009
Completion date April 2011
View Details
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