Periapical Diseases Clinical Trial
Official title:
Efficiency of Diode Laser in Control of Post-endodontic Pain (A Randomized Clinical Trial )
Study is a Randomized clinical trial conducted at Endodontic department- Ain Shams university
Cairo. Egypt.
180 eligible patients were selected and included in the study to assess the post-endodontic
pain of diode laser activated irrigation versus soft tissue diode laser application post
obturation versus conventional root canal treatment .
Sample size is 180 180 Patients were randomly distributed in 3 groups , one group of patients
received laser therapy after root canal treatment and the other group received disinfection
by Diode laser activated irrigation , the third group received no treatment just conventional
Root canal treatment. • Patients were equally divided into 3 groups (n=60 in each group ) The
study in a Single blinded Randomized clinical trial
, Numbers for patients will be generated and distributed randomly in a table on an Excel
sheet, and in front of each number either a letter (C) for control or (I) for intervention
will be typed After patients were selected in the study they will be asked to fill in a
consent form , that states that they are part of a clinical trial and that they may or may
not have a laser session following root canal treatment to test its ability to control pain ,
the consent will also require them to take a questionnaire at home to measure their pain
level and they were willingly do it.
Conventional root canal treatment were done to selected teeth , and any cases with procedural
errors were excluded.
Group A Laser activated irrigation :Disinfection were done by using 5 ml of 2.5% sodium
hypochlorite irrigation for 1 minute. Irrigation will be performed with a 30-gauge needle
side vented The irrigation needles were introduced passively up to 2 mm away the working
length. After irrigation Laser treatment will be performed with a diode laser, at a
wavelength of 980 nm with a repeated pulse mode using a pulse duration of 5s per canal and a
pulse interval of 0.2 ms. The laser irradiation were delivered for 1 minute into the canal up
to 1 mm short of the working length, with circling movements from the apical part moving
towards the coronal part Group B Soft tissue laser application : Endodontically treated teeth
were targeted by virtue of a dental applicator positioned at a right angle to the mucosa at
the level of the apices. Application of the laser probe were applied to both the buccal and
lingual mucosae overlying the apices of the target tooth. Total exposure time for each tooth
was 60 seconds (a dose = 70 j/cm2 for analgesia) by the co-investigator The laser unit used
in this study will be a diode laser (Lite Medics 1.00 Watt serial number 148 Ver.SwvM.
150VS108VT.100) of wavelength 980nm and Max power 15 WCW Class IV Laser Product ) in
continuous wave mode Group C : conventional root canal treatment : no laser intervention
Patients were instructed to record their post-endodontic pain by VAS where 0 stands for no
pain and 10 stands for severe pain.
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