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Oxycodone-Naloxone in Relieving Opioid-Related Constipation
This study is ongoing, but not recruiting participants.
First Received: December 14, 2006   Last Updated: April 29, 2008   History of Changes
Sponsored by: Mundipharma Research GmbH & Co KG
Information provided by: Mundipharma Research GmbH & Co KG
ClinicalTrials.gov Identifier: NCT00412152
  Purpose

The primary objective of this study is to demonstrate that subjects with moderate to severe non-malignant pain taking oxycodone/naloxone prolonged release tablets have improvement in symptoms of constipation compared to subjects taking oxycodone prolonged release tablets alone.


Condition Intervention Phase
Pain
Drug: Oxycodone nalaxone prolonged release tablets (OXN)
Phase III

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: A Randomised, Double-Blind, Parallel-Group, Multicentre Study to Demonstrate Improvement in Symptoms of Constipation in Subjects With Non-Malignant Pain Taking Oxycodone Equivalent of >20 mg/Day and <50 mg/Day as Oxycodone/Naloxone Prolonged Release Compared to Subjects Taking Oxycodone Prolonged Release Tablets Alone.

Resource links provided by NLM:


Further study details as provided by Mundipharma Research GmbH & Co KG:

Primary Outcome Measures:
  • To demonstrate that subjects with moderate to severe non-malignant pain taking oxycodone/naloxone prolonged release tablets have improvement in symptoms of constipation compared to subjects taking oxycodone prolonged release tablets.

Study Start Date: January 2006
Estimated Study Completion Date: April 2008
Detailed Description:

Patients with a documented history of moderate to severe non-malignant pain that require around the clock opioid therapy will be randomised to an oxycodone or an oxycodone-naloxone treatment arm to assess the safety and efficacy of oxycodone/naloxone prolonged release compared to oxycodone prolonged-release in relieving opioid-related constipation.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Male or female subjects at lest 18 years or older with pain.
  • Subjects must report constipation caused or aggravated by opioids.

Exclusion Criteria:

  • Females who are pregnant or lactating.
  • Subjects with evidence of significant structural abnormalities of the gastrointestinal (GI) tract (e.g.

bowel obstruction, strictures).

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00412152

Sponsors and Collaborators
Mundipharma Research GmbH & Co KG
Investigators
Principal Investigator: Karen Simpson, MBChB Seacroft Hospital, Pain Management Services, L Ward, York Road, Leeds
  More Information

No publications provided by Mundipharma Research GmbH & Co KG

Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
Study ID Numbers: OXN3001, 2005-002398-57
Study First Received: December 14, 2006
Last Updated: April 29, 2008
ClinicalTrials.gov Identifier: NCT00412152     History of Changes
Health Authority: United Kingdom: Research Ethics Committee

Keywords provided by Mundipharma Research GmbH & Co KG:
A randomised
double blind
parallel group
multicentre study to demonstrate improvement in symptoms of constipation in subjects with non malignant pain
Moderate to severe chronic non-malignant pain

Study placed in the following topic categories:
Signs and Symptoms
Signs and Symptoms, Digestive
Oxycodone
Constipation
Central Nervous System Depressants
Narcotics
Pain
Peripheral Nervous System Agents
Analgesics
Analgesics, Opioid
Naloxone

Additional relevant MeSH terms:
Signs and Symptoms, Digestive
Oxycodone
Physiological Effects of Drugs
Central Nervous System Depressants
Narcotics
Pharmacologic Actions
Signs and Symptoms
Sensory System Agents
Therapeutic Uses
Constipation
Analgesics
Peripheral Nervous System Agents
Central Nervous System Agents
Analgesics, Opioid

ClinicalTrials.gov processed this record on September 11, 2009