CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 122 enrolled
Drug / intervention
Brufen retard +2 moredrug
Likely dose
Brufen retard 800mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00895843
NCT00895843N/ACompleted
CompareCT.gov

Protective Analgesia Using Bupivacaine and Conventional Release Ibuprofen Versus Bupivacaine and Sustained Release Ibuprofen for Postoperative Pain Relief in Patients Undergoing Third Molar Surgery: a Randomised Controlled Trial

University of Manchester·interventional·Posted May 8, 2009·Updated Jun 1, 2009

In Brief

A clinical study evaluating Brufen retard, ibuprofen, and 1 other intervention for Postoperative Pain and Wisdom Tooth. Completed, enrolled 122 participants across 2 sites.

Detailed Summary

The purpose of this study is to investigate whether robust analgesic regime (protective analgesia) can improve postoperative pain experience for patients undergoing lower wisdom teeth extraction under day case general anaesthetic.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsPostoperative Pain, Wisdom Tooth
CountriesUnited Kingdom
CollaboratorsManchester University NHS Foundation Trust

Timeline

N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 8, 2009
Enrollment StartNov 1, 2006
Primary CompletionDec 1, 2007
Study CompletionJan 1, 2008
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 17.2 years ago

Interventions

Brufen retarddrug

Single dose 2 x 800mg tablets 2 hours prior to surgery

ibuprofendrug

Single dose ibuprofen 2 x 200mg tablets 2 hours prior to surgery

Bupivacainedrug

Up to 10ml of Bupivacaine 0.5% with 1:200,000 Adrenaline given prior to surgical incision as inferior alveolar nerve block and long buccal nerve infiltration.