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A Comparison of Oxycodone/Naloxone and Oxycodone After Laparoscopic Hysterectomy

Postoperative Pain Clinical Trial

Clinical Trial Summary

Objectives:

Primary objective:

- To demonstrate that the treatment with OXN PR tablets up to 72 hrs after surgery is superior to the treatment with OxyPR with regards to constipation in subjects with postoperative pain after laparoscopic hysterectomy based on interviews 24h, 72 h and 1 week postoperatively.

The secondary objectives:

- Analgesic effect (including registration during the first 24 hrs)

- To asses the frequency of pain rescue mediation use (in the double-blind phase, 0-72 hrs)

- Frequency of nausea and vomiting

- Frequency of other adverse events

- Appetite

- Mobilization

The exploratory objectives:

- Overall patient satisfaction at 24, 72 hrs and 1 week

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01109511
Study type Interventional
Source Oslo University Hospital
Contact
Status Completed
Phase Phase 4
Start date March 1, 2010
Completion date July 30, 2011
View Details
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