Orthodontic Appliance Complication
Conditions
Keywords
Pain
Brief summary
To compare the analgesic property of acupressure with NSAIDs (Ibuprofen) in controlling pain following orthodontic treatment. This will be achieved by assessing the effectiveness of acupressure in controlling pain and discomfort by measuring the degree of pain relief after bonding of brackets to teeth and placement of initial archwire.
Detailed description
Single centred randomised controlled trial with subjects recruited from a hospital orthodontic outpatient department in Dundee Dental Hospital. If informed consent is obtained, then the subject details will be delivered to the trial coordinator for randomisation to one of the groups, NSAIDs or acupressure group. All subjects who are eligible for inclusion will be advised of the nature and purpose of the trial. The total number of subjects recruited will be approximately 36 with the acupressure and NSAID group containing approximately 18 subjects each. All subjects who meet the inclusion criteria will be informed of the study and written consent sought for their participation. Subjects will be recruited from the new patient clinics and routine treatment waiting list. . The subjects will be asked to measure the level and duration of pain and discomfort using a pain diary to record their experiences using visual analogue scales (VAS). The pain diary will be completed from 4 hours to 7 days after treatment after the insertion of the first orthodontic aligning archwire. Intervention Groups In the acupressure group the subjects will be given an advice sheet and advised to use a definitive acupressure point on the back of the hand region to control orthodontic pain. In the NSAID group the subjects will be given an advice sheet and advised to take Ibuprofen for the orthodontic pain Pain scores via VAS will be analysed at 4hours, 24 hours, and 7 days after the orthodontic treatment. The VAS consists of a horizontal line, 100 mm in length with descriptive words at each end of the line which act as anchors e.g. no pain, great pain. The patient marks on the line the point that they feel represents their perception of their current state. The VAS score is determined by measuring in millimetres from the left hand end of the line to the point that the patient marks
Interventions
BEHAVIORALAdvice sheet
Advice on management of post orthodontic pain
Sponsors
NHS Tayside
University of Dundee
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
Not possible to mask due to nature of intervention except for outcome assessor
Intervention model description
Randomised parallel clinical trial
Eligibility
Sex/Gender
ALL
Age
12 Years to 25 Years
Healthy volunteers
No
Inclusion criteria
* aged 12-25 * malocclusion requiring treatment * scheduled to begin orthodontic treatment * requires fixed orthodontic braces on upper and lower teeth.
Exclusion criteria
* previous orthodontic treatment * current use of analgesics * contraindications to the use of NSAIDs * previous acupressure experience * pregnant
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain experience | 7 days | Visual analogue scale |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Impact of pain on sleep | 7 days | Impact of pain on sleep as recorded in pain diary |
| Impact of pain on eating | 7 days | Impact of pain on eating as recorded in pain diary |
| Rescue medication | 7 days | Need to use rescue medication to manage pain as recorded in pain diary |
Countries
United Kingdom
Outcome results
None listed