About this trial
Aims: The purpose of this randomized clinical trial is to assess and compare the post operative pain, swelling and quality of life after endodontic microsurgery using either conventional osteotomy or piezoelectric osteotomy . The PICO question that will be used is Does endodontic microsurgery using piezoelectric osteotomy have similar clinical performance in terms of post operative pain and swelling to that of endodontic microsurgery using conventional hand-piece osteotomy.
Material and methods:
based on solid inclusion criteria , a total of 44 patients in need of endodontic microsurgery will be randomly distributed into two groups (n=22) according to the osteotomy technique: conventional and piezoelectric osteotomy. A standardized microsurgical technique will be employed. After the microsurgery procedure, a pain questionnaire that contain visual analogue scale will be given to each patient to evaluate the pain incidence and intensity at 5 time intervals, 24 hours, 48 hours, 72 hours, 96 hours and 120 hours. The patients will be recalled as well, at days 2 and 7 to evaluate the swelling. Statistical analysis will be performed using chi-square test and linear regression analysis.
Eligibility criteria
Qualifiers
Non-smokers .
Teeth that are periodontally healthy.
Age (18-65)
Disqualifiers
Patients with an active systematic diseases that may affect the outcome
Medically compromised patients on long term medications.
Patients who had received analgesics or antibiotics prior to surgery will be postponed.
Cases where orthograde endodontic treatment is feasible
Trial design
Treatments tested in this trial
- Endodontic Microsurgery
Treatment groups
Sponsors and collaborators
King Abdullah University Hospital
Lead sponsor
Jordan University of Science and Technology
Collaborator