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Clinical Efficacy of a New Piezoelectric Technique for Wisdom Teeth Extraction

A

Azienda Ospedaliera di Bolzano

Status

Unknown

Conditions

Impacted Third Molar Tooth

Treatments

Procedure: conventional extraction
Procedure: piezoelectric extraction

Study type

Interventional

Funder types

Other

Identifiers

NCT03619460
0060125-BZ

Details and patient eligibility

About

the aim of this randomized controlled clinical study is to evaluate the efficacy of a new piezoelectric technique for wisdom teeth extraction without using manual tools versus the conventional one.Patients referred to the hospital of Bolzano for wisdom tooth extraction will be randomly divided in two groups. In the test group all the procedure will be performed using piezoelectric instruments, while in the control one conventional manual instruments will be used. Main outcome measures are patient pain and complications, secondary outcome measures are duration of the surgical treatment and soft tissue healing

Full description

Wisdom teeth extraction can be difficult and patient can suffer post operative swelling and pain. A new piezoelectric technique for wisdom teeth extraction was developed and it showed promising results in terms of surgical effectiveness and patients post operative complications. The aim of the study is to compare the new technique with special designed piezoelectric tools with the traditional one in a randomized controlled way. The same procedures are to be followed for teeth extraction except for the use of a piezoelectric lever in one group and a manual lever in the other one. The study is a mono-center, pragmatic, randomised clinical trial (RCT) of parallel group design. The trial would have one week follow up. All patients referred to the Dental Department of S.Maurizio Hospital (Bolzano, Italy) for the extraction of wisdom teeth are considered eligible for the study.

Enrollment

44 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients referred for wisdom tooth extraction
  • Patients older than 18 years old and able to sign the informed consent

Exclusion criteria

  • General contraindications to surgery.
  • Patients irradiated in the head and neck area.
  • Immunosuppressed or immunocompromised patients.
  • Patients who took or are taking bisphosphonates intravenously.
  • Uncontrolled diabetes
  • Presence of oral pathologies that seriously involved oral mucosa
  • Patients with poor oral hygiene and motivation.
  • Patients with oral pathologies with serious mucosal involvement
  • Pregnancy or lactation.
  • Addiction to alcohol or drugs.
  • Psychiatric problems.
  • Patients with an acute infection inflammation around the tooth to be extracted.
  • Wisdom teeth with roots attached or positioned around the nerve
  • Patients unable to come to the required follow up visits

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

44 participants in 2 patient groups

piezoelectric extraction
Experimental group
Description:
The flap will be raised using a Piezoelectric elevator, the eventual bone around the third molar crown will be removed with the same piezoelectric lever used for luxation and root extraction. The eventual rizectomy will be performed using a piezoelectric saw.
Treatment:
Procedure: piezoelectric extraction
conventional extraction
Active Comparator group
Description:
The flap will be raised using a manual elevator and the eventual bone around the third molar crown will be removed with a bone bur with a straight handpiece while the eventual rizectomy will be performed using a bone bur. Manual levers will be used for luxation and tooth extraction
Treatment:
Procedure: conventional extraction

Trial contacts and locations

1

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Central trial contact

MARIA GABRIELLA GRUSOVIN, DDS; TOMASO VERCELLOTTI, MDS

Data sourced from clinicaltrials.gov

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