Clinical Trials Directory

Trials / Completed

CompletedNCT01672112

Comparison of the Efficacy of Oral Oxycodone and Oral Codeine in the Treatment of Postcraniotomy Pain

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Tan Tock Seng Hospital · Academic / Other
Sex
All
Age
21 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The efficacy of codeine is dependent on its demethylation to morphine. This extent of demethylation has wide inter-individual variability, making codeine's efficacy as a analgesic variable. Oxycodone is a semi-synthetic opioid and is a weak agonist on mu opioid receptors. Codeine has been the mainstay of analgesia for patients after craniotomy for many years. Traditionally, craniotomies were not thought to be very painful procedures, hence the use of codeine, a moderately potent opioid (when compared to morphine). However, in recent years, it has been found that up to 70% of post-craniotomy patients have moderate to severe pain and codeine did not provide adequate analgesic relief. Many studies have compared codeine to other drugs such as PCA morphine, fentanyl and tramadol, and patients on these stronger opioids generally had lower pain scores and better satisfaction. No study has been conducted to determine the efficacy of analgesia of oral oxycodone to oral codeine. Hence, the hypothesis is that oxycodone is more effective than codeine in providing pain relief in post-craniotomy patients.

Conditions

Interventions

TypeNameDescription
DRUGOxycodoneOral Oxycodone 5mg 6hrly/prn
DRUGCodeineOral Codeine 60mg 6hrly/prn

Timeline

Start date
2012-07-01
Primary completion
2015-01-01
Completion
2015-01-01
First posted
2012-08-24
Last updated
2015-05-15

Locations

1 site across 1 country: Singapore

Source: ClinicalTrials.gov record NCT01672112. Inclusion in this directory is not an endorsement.