Skip to content

3D Evaluation of Facial Swelling Post Impacted Lower Third Molars Surgery: RCT

Three-dimensional Facial Swelling Evaluation of Piezo-electric Versus Conventional Drilling Bur Surgery of Impacted Lower Third Molar: a Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05488028
Enrollment
22
Registered
2022-08-04
Start date
2020-09-01
Completion date
2021-04-30
Last updated
2022-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impacted Third Molar Tooth, Swelling/ Edema

Keywords

piezosurgery, conventional osteotomy, impacted lower third molar, facial scan, 3d rendering

Brief summary

Aim of the study is to evaluate the swelling following the osteotomy when performed with drilling bur versus piezo-electric instrument in the mandibular impacted third molar extraction, using a facial reconstruction software

Interventions

PROCEDUREPiezo-electric surgery of impacted lower third molars

During lower third molar surgery, osteotomy is performed using piezoelectric instrumentation. When necessary, tooth sectioning was performed with a high-speed tungsten carbide slit drill under saline irrigation and the tooth removed in single or multiple segments.

PROCEDURERotary bur surgery of impacted lower third molars

During lower third molar surgery, osteotomy is performed using rotary instruments

Sponsors

Azienda Ospedaliera Universitaria Policlinico G. Martino
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Intervention model description

Split-mouth model

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* good general health conditions; * presence of bilateral and symmetrical impacted third molars (according to the classifications of Winter and Pell and Gregory);

Exclusion criteria

* no clinical evidence of major facial asymmetry; * use of medication that would influence or alter wound healing; * temporomandibular joint disorder history; * smoking

Design outcomes

Primary

MeasureTime frameDescription
Facial swelling7 daysT0-T1 and T0-T2 scans are opened and superimposed through three reference points: endocanthion left (inner most point on commissure of left eye fissure), endocanthion right (inner most point on commissure of right eye fissure) and subnasale (mid point of columella). After matching, the swelling was calculated by selecting the area of the swelling and subtracting the two images.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026