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A Non-interventional, Observational Study for Targinact® Treatment in Patients With Severe Pain.

NCT01983137 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1338

Last updated 2013-11-13

No results posted yet for this study

Summary

This non-interventional, observational study evaluates the efficacy of Targinact with regard to pain relief in daily clinical practice in Belgium compared to the previous analgesic treatment.

Conditions

  • Severe Pain

Interventions

DRUG

Targinact® (oxycodone/naloxone)

Sponsors & Collaborators

  • Mundipharma CVA

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2012-12-31
Completion
2012-12-31

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01983137 on ClinicalTrials.gov