Actively Recruiting
Postoperative Symptoms Following Endodontic Microsurgery
Led by King Abdullah University Hospital · Updated on 2025-04-08
40
Participants Needed
1
Research Sites
186 weeks
Total Duration
On this page
Sponsors
K
King Abdullah University Hospital
Lead Sponsor
J
Jordan University of Science and Technology
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Postoperative Symptoms Following Endodontic Microsurgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Non-smokers
- Teeth that are periodontally healthy
- Age between 18 and 65 years
You will not qualify if you...
- Patients with active systemic diseases that may affect the outcome
- Medically compromised patients on long term medications
- Patients who received analgesics or antibiotics prior to surgery
- Cases where orthograde endodontic treatment is feasible
- Teeth with poor prognosis
- Teeth with active periodontal disease (pocket depth > 5 mm)
- Emotionally distressed patients
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Trial Site Locations
Total: 1 location
1
Jordan University of Science and Technology
Irbid, Jordan, POBOX 3030
Actively Recruiting
Research Team
L
Lama A Awawdeh, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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