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Trial registered on ANZCTR
Registration number
ACTRN12616001087448
Ethics application status
Approved
Date submitted
24/06/2016
Date registered
11/08/2016
Date last updated
11/08/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Does a topical anesthetic gel work better than infiltration anesthesia for ultrasonic scaling procedures? A split mouth, double blinded randomised controlled trial.
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Scientific title
Does a topical anesthetic gel work better than infiltration anesthesia for ultrasonic scaling procedures? A split mouth, double blinded randomised controlled trial.
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Secondary ID [1]
289508
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nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
peridontitis
299209
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Gingivitis
299485
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Condition category
Condition code
Oral and Gastrointestinal
299218
299218
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Anaesthesiology
299383
299383
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0
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Anaesthetics
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
This will be a split mouth study. An independent researcher "I" makes random allocation
cards using computer-generated random numbers. He keeps the original random allocation sequences in an inaccessible third place and works with a copy. He will open the envelop for every patient at start of treatment and will tell dr A that which quadrant gets which form of intervention.
. 1.7 gram of 5 % lidocaine and prilocaine gel will be applied by dental surgeon in form of the topical dental cartridge which will applied with 23 guage blunt tipped applicator in the three teeth (central incisor, lateral incisor and canine). the quadrant will be chosen by computer generated random allocation by dr I. This dose will be spread between the specified teeth in quadrant.
Lidocaine infiltration anesthesia will be given in the central incisor, lateral incisor and canine ( the quadrant will be chosen by computer generated random allocation by dr I)..1.8 ml cartridge of 2% lidocaine with 1:100,000 epinephrine will be spread in specified teeth in form of infiltration by dental surgeon. Only single dose of both above anesthetics will be given to one patient.
The central incisor, lateral incisor and canine of two quadrants will serve as a control with saline wash given in both of them( the quadrant will be chosen by computer generated random allocation by dr I)
After local anesthesia has been given to the patients by Dr A, Dr B and Dr C will perform the ultrasonic scaling procedures. Both Dr B and Dr C will be blinded to the control and anesthesia quadrants.Dr A will check the time taken for the anesthesia to be effective with the blunt end of perisoteal elevator. After every 30 seconds the time will be noted for all four quadrants. The Dr X (who is also blind to the anesthetic applied in all quadrants) will ask the patient about the pain levels using a Visual Analogue Scale (VAS) calibrated from 1 to 10 at the start of treatment and at the end of treatment.
Both of the anesthesia will be given simultaneously. The anesthetic gel is effective for 20 minutes and infiltration for 40 minutes. During the procedure doctor Z will be observing the patient according to SEM scale which is sound eyes and motor scale
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Intervention code [1]
295096
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Treatment: Drugs
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Comparator / control treatment
Saline wash will be given in central incisor, lateral incisor and canine ( the quadrant will be chosen by computer generated random allocation by dr I)
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Proportion of participants with a reduction in pain scores using visual analogue scale
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Assessment method [1]
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Timepoint [1]
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one hour after the commencement of intervention
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Secondary outcome [1]
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Difference in time taken for topical and infiltration anaesthesia to be effective, assessed by the dental surgeon checking the time taken by anesthetic to be effective with the blunt end of the perisoteal elevator and writing in the study log
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Assessment method [1]
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Timepoint [1]
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Every 30 seconds from application of anaesthesia to time of no sensation in upper and lower right and left central incisor, lateral incisor and canine with blunt end of perisoteal elevator
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Eligibility
Key inclusion criteria
1. All participants must require ultrasonic scaling in all four mouth quadrants .
2. Patients who have not undergone any periodontal therapy in the past 12 months
3. Patients having a minimum of two incisors, one canine, one premolar and one molar in each quadrant
4. Patients between the ages of 20 and 60 years
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Minimum age
20
Years
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Maximum age
60
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
(1) Patients requiring prophylactic antibiotics before periodontal probing
(2) Patients suffering from any mental disorders or with any chronic pain problems
(3) Patients suffering with coagulation/bleeding disorders or on anticoagulants
(4) Pregnant or lactating women
(5) Patients with congenital or idiopathic methemoglobinemia
(6) Patients reporting hypersensitivity to lidocaine/benzocaine
(7) Patients taking nonsteroidal anti-inflammatory drugs in the 3 days before participation in the study and
(8) Patients having acute periodontal pain, pulpitis, abscesses, or other acute infections.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
vas scale
sem scale will be used to assess outcomes
The sample size was calculated using the repeated measures ANOVA design . A VAS variance as reported for anesthetics was 3 and for intergroup variance was 14. Errors were set as alpha =0.05 and beta=0.2. A total sample size was determined to be 20 patients in order to compensate for possible dropouts . The level for statistical significance is 0.05
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/09/2016
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
20
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
7977
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Pakistan
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State/province [1]
7977
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Islamabad
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Riphah Academy of Research and Education
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Address [1]
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Riphah Academy of Research and Education
Islamic International Medical College
274 Peshawar road, Old supreme court building Rawalpindi, Pakistan.
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Country [1]
293879
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Pakistan
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Primary sponsor type
Individual
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Name
Humza Bin Saeed
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Address
Islamic International Dental College, 7TH Avenue, G-7/4, Islamabad, Pakistan
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Country
Pakistan
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Secondary sponsor category [1]
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Individual
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Name [1]
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Kinza Ayub
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Address [1]
292714
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Islamic International Dental College, 7TH Avenue, G-7/4, Islamabad, Pakistan
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Country [1]
292714
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Pakistan
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
295307
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Islamic International Dental College Research Ethics Committee
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Ethics committee address [1]
295307
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Islamic International Dental College, 7TH Avenue, G-7/4, Islamabad, Pakistan
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Ethics committee country [1]
295307
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Pakistan
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Date submitted for ethics approval [1]
295307
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15/05/2016
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Approval date [1]
295307
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14/06/2016
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Ethics approval number [1]
295307
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IIDC/IRC/2016/06/003
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Summary
Brief summary
This study will aim to evaluate the efficacy of anesthetic gel in comparison to infiltration and saline (placebo) during the scaling procedure. Controlling the sensation of pain and the associated anxiety is of prime importance in the practice of dentistry. Dental pain and its associated anxiety has been identified as one of the two most important barriers to dental access. A range of treatments, including pharmacological and non-pharmcalogical interventions have been advocated for the management of pain and anxiety in dentistry.Periodontal diseases are amongst the most common reported dental ailments. Majority of people are reported to be suffering from some form of periodontal diseases. The most common management strategy adopted for mild to moderate periodontal diseases is ultrasonic scaling. Patients have reported undergoing varying levels of pain while undergoing scaling procedures. Several strategies have been reported in literature to manage pain associated with scaling. These include the use of infiltration and topical local anesthesia. More recently, a new non-injection anesthetic, lidocaine/prilocaine gel for scaling and root planning has also been introduced. Moreover, it has recently been demonstrated that a eutectic mixture of local anesthetics (EMLA) is more efficient than a lidocaine gel. There is varying evidence in literature comparing the efficacy of topical versus infiltration local anesthesia for scaling procedures. Our study aims to assess the clinical anesthetic efficacy of lidocaine and prilocaine topical gel versus lidocaine infiltration injection and saline (placebo) for the management of pain during scaling procedures in patients with mild to moderate periodontal disease.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Humza Bin Saeed
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Address
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Islamic International Dental College, 7TH Avenue, G-7/4, Islamabad, Pakistan
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Country
66426
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Pakistan
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Phone
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+92512891835
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Fax
66426
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Email
66426
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[email protected]
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Contact person for public queries
Name
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Humza Saeed
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Address
66427
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Islamic International Dental College, 7TH Avenue, G-7/4, Islamabad, Pakistan
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Country
66427
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Pakistan
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Phone
66427
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+92512891835
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Fax
66427
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Email
66427
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[email protected]
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Contact person for scientific queries
Name
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Humza Saeed
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Address
66428
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Islamic International Dental College, 7TH Avenue, G-7/4, Islamabad, Pakistan
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Country
66428
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Pakistan
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Phone
66428
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92512891835
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Fax
66428
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Email
66428
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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