Topical Modification of Dental Pain and Movement

Phase 3

Recruiting

• Conditions: Pain; Widsom tooth removal; Anaesthesiology - Pain management; Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

• Registration Number: ACTRN12619001167156
• Lead Sponsor: Professor Peter Smith

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-08-20
• Last Update Posted: 28 March 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Patients undergoing bilateral wisdom tooth extraction, 14 years and over.

Exclusion Criteria

Patients with an intolerance to the spray, allergic reaction to spray/placebo ingredients, intellectually disabled participants and persons that speak languages other than English.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain will be assessed using a 10 point Likert scale, where patients grade their pain from 0 (no pain) to 10 (worst possible pain). [Day 1, 2, 3, 4 and 5 (primary timepoint). ];Maximal mouth opening.<br><br>This will be measured by the patient opening their mouth to its maximal capacity and using a cardboard ruler (provided to the patient) to measure the maximal width. [Day 1, 2, 3, 4, 5 (primary timepoint). ]

Secondary Outcome Measures

Name	Time	Method
Medication use for analgesia following wisdom tooth extraction. This will be assessed using a study-specific questionnaire requiring a list of additional pain relief used following wisdom tooth surgery and any regular analgesia e.g. that required for other medical conditions. [Day 1, 2, 3, 4 and 5.]