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Completed

NCT Number: NCT05684601

Impact of 3D Intraoral Scanning on Postsurgical Evaluation of Mandibular Third Molar Surgery

The aim of this study was to analyze the effectiveness of piezoelectric surgery and traditional rotating device in reducing perioperative sequelae after impacted mandibular third molar surgery in 56 subjects. Ni All subjects were randomly allocated to receive one treatment.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

AOU Policlinico G. Rodolico

Catania, 95124, Italy

About this study

The aim of this study was to analyze the effectiveness of piezoelectric surgery and traditional rotating device in reducing perioperative sequelae after impacted mandibular third molar surgery. Fifty-six patients who needed surgical extraction of an impacted mandibular third molar were selected for the study. All subjects were randomly allocated to receive one of the following surgical treatments piezoelectric surgery (n = 28), traditional surgery with rotating device (n = 28). The primary outcome was postoperative pain, evaluated using the visual analogue scale (VAS) score at baseline, 1, 2, 5, 7, 10 and 14 and 28 days following surgery. The secondary outcomes chosen were changes in postoperative swelling and maximum mouth opening values compared to preoperative ones.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • aged between 18 and 32 years;
  • good general health;
  • the presence of one impacted third molar in the mandible with a class II position, type B impaction;
  • absence of pericoronitis or signs of inflammation during the last 30 days. Panoramic radiographs were used to determine tooth position.

Exclusion criteria

  • the presence of any systemic disease;
  • consumption of oral contraceptives or other medications;
  • consumption of any immunosuppressive or anti-inflammatory drugs during the 3 months prior to the study;
  • status of pregnancy or lactation;
  • previous history of excessive drinking;
  • allergy to local anesthetic;
  • smoking habit.

Treatment and study plan

Third molar surgery

Device

It was extracted one impacted mandibular third molar per patient with piezoelectric or rotating drills device

Primary outcomes

  1. Visual analogue Scale (VAS), values 1-10

    Time frame: 1- and 3-months

    Evaluation of VAS value changes at baseline and follow-up session

Sponsors and collaborators

Lead sponsor

University of Catania

Other

Registry information

Official study title

Analysis Impact of 3D Intraoral Scanning on Postsurgical Evaluation of Mandibular Third Molar Surgery Using Piezosurgery Versus Traditional Rotating Instrumentations

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Jan 13, 2023
Registry last updated
Jan 13, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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