Actively Recruiting
Comparison of Piezoelectric and Traditional Surgery for Lower Third Molar Germectomy Assessment of Post-Operative Swelling and Outcomes
Led by Amerigo Giudice · Updated on 2025-01-16
22
Participants Needed
1
Research Sites
65 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effects of two surgical methods, piezoelectric surgery and the traditional technique, on soft tissue swelling in patients undergoing bilateral removal of lower third molars (germectomy). The study focuses on comparing post-operative facial swelling using detailed photographic scanning technology to measure changes after surgery. This comparison aims to better understand how these techniques affect recovery from tooth removal. Participants will undergo bilateral germectomy of their lower third molars using either the piezoelectric technique or the traditional surgical method. Both procedures will be applied as part of the treatment, allowing researchers to observe differences in swelling between the two approaches. The soft tissue swelling after surgery will be monitored and measured using a photogrammetry facial scanner called Marathon MT-4000. During the study, participants will have their facial swelling assessed qualitatively and quantitatively by measuring volumetric and linear changes compared to before surgery. These measurements will be taken at two days and seven days after the surgery to track swelling progression. The total participation involves pre-surgical evaluation, surgery using one of the two techniques, and follow-up assessments to monitor post-operative swelling and recovery.
CONDITIONS
Official Title
Comparison of Piezoelectric and Conventional Surgery for Germectomy of the Lower Third Molar
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 14 and 24 years, with both lower third molars in the developmental stage (with incompletely formed roots) and requiring extraction of both for prophylactic, therapeutic or strategic reasons
- Good quality of radiographic investigations (CBCT)
- Good health status
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
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Trial Site Locations
Total: 1 location
1
Magna Graecia University of Catanzaro
Catanzaro, Italy, 88100
Actively Recruiting
Research Team
A
Amerigo Giudice, Prof, MD, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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