The role of peri-operative gabapentin in the management of pain following tonsillectomy
Phase 3
- Conditions
- Pain following tonsillectomyPost-tonsillectomy analgesic consumptionPost-tonsillectomy nauseaPost-tonsillectomy vomitingPost-tonsillectomy return to normal activityPost-tonsillectomy return to normal dietSurgery - Other surgeryAnaesthesiology - Pain management
- Registration Number
- ACTRN12613000663752
- Lead Sponsor
- Department of Surgical Sciences, University of Otago
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Participants will be aged 16 years and over, scheduled for elective tonsillectomy between January 2014 and December 2014
Exclusion Criteria
Exclusion criteria will include contraindications to gabapentin, other concurrent procedures, revision or unilateral tonsillectomy, inability to complete the scoring charts, and those with suspected malignancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measure is post-operative pain.[This will be assessed using a VAS, scoring at 2, 4, and 6 hours following surgery and on post-operative days 1 to 14.]
- Secondary Outcome Measures
Name Time Method Secondary outcomes will be post-operative analgesic consumption.[This will be assessed on post-operative days 1 to 14 by way of a questionnaire and recovery of un-used analgesia at the end of the 2 week period.];Post-operative nausea[Days 1-14 assessed by validated Postoperative Nausea and Vomiting (PONV) Intensity Scale.];Post-operative vomiting[Days 1-14 assessed by validated Postoperative Nausea and Vomiting (PONV) Intensity Scale.];Post-operative return to normal activity.[Indication by non-validated questionnaire developed specifically for this study of day return to normal activity (From days 1-14).];Post-operative return to normal diet.[Indication by non-validated questionnaire developed specifically for this study of day return to normal diet (From days 1-14).]