Effect of Piezoelectric Device on Intraoperative Hemorrhage Control and Quality of Life

Periapical Lesion Clinical Trial

Official title:

Effect of Piezoelectric Device on Intraoperative Hemorrhage Control and Quality of Life After Endodontic Microsurgery in Maxillary Molar Teeth: a Randomized Controlled Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT06240182
• Other study ID #: Yamini kindra
• Status: Active, not recruiting
• Phase: N/A
• Start date: November 1, 2022
• Est. completion date: May 1, 2024

Study information

• Verified date: January 2024
• Source: Postgraduate Institute of Dental Sciences Rohtak
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Most osteotomies and apicoectomies in periapical surgeries are performed by surgical carbide or diamond burs. But greater pressure is applied during cutting which causes more thermal and mechanical damage to the bone. Also, when it comes in contact with soft tissues like nerves or vessels it results in profuse bleeding which affects vision in surgery and neurosensory disturbance at a later stage along with the deposition of metal shavings and bony particles resulting in impaired healing. The main advantages of piezoelectric surgery in various studies are highlighted as selective hard tissue cutting and sparing soft tissue, so even if it comes in contact with vessels, nerve or Schneiderian membrane it does not result in profuse bleeding, postoperative nerve damage or perforation.

Description:

Most periapical radiolucent lesions heal uneventfully after endodontic treatment. However, some cases may require periradicular surgery in order to remove pathologic tissue from the periapical region and simultaneously eliminate any source of irritation that could not be removed by orthograde root canal treatment

In dentistry, the piezoelectric bone surgery was developed by the oral surgeon Tomaso Vercellotti in 1988, to overcome the limitations of traditional instrumentation, which was first used for maxillary sinus surgery to reduce the incidence of Schneiderian membrane perforations.

Piezoelectric surgery is a promising technical modality with applications in several aspects of endodontic surgery like bone-tissue management, enucleation of radicular cysts, root-end resection & root-end Cavity Preparation. Piezoelectric surgical device operates with principles similar to the piezoelectric dental scaler devices except for its power which is three to six times higher than the piezoelectric dental scalers. The advantages of piezoelectric surgery over conventional endodontic surgery include protection of soft tissues, optimal visualization of the surgical field, decreased blood loss, reduced vibration and noise, increased patient comfort and protection of tooth structures. But some of its disadvantages are initial financial burden for setting up of the unit, long duration of surgery and instruction manuals discouraging its use in patients with cardiac pacemakers.

Less intraoperative blood loss and less chance of inferior alveolar nerve injury was observed on piezoelectric osteotomy in orthognathic surgery at no extra time investment.

In a similar study comparing piezo osteotomy and traditional saw in bimaxillary orthognathic surgery there was significantly reduced blood loss, postoperative hematoma, swelling and nerve impairment in piezo osteotomy but the mean operative time was more

Distance of 1.97mm between the maxillary sinus floor and root apices and even shorter distance between the periapical lesion and maxillary sinus floor warns the surgeon during removal of lesion.

Schneiderian membrane perforation rate while performing lateral window sinus elevation procedure reduced from 30% by conventional surgical burs to 7% by piezoelectric unit.

The capacity of selective cutting, reducing the risk of perforating the sinus lining, and increased visibility of the surgical field due to the cavitation effect from the saline irrigating solution of the piezoelectric unit makes it the preferred option for performing upper molar surgery.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 30
• Est. completion date: May 1, 2024
• Est. primary completion date: April 1, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 16 Years to 55 Years

Eligibility

Inclusion criteria:

1. Patients between 16-55 years of age

2. ASA-1 or ASA- 2 according to the classification of the American Society of Anesthesiologists)

3. Peri radicular lesion of strictly endodontic origin with size of lesion = 5mm in CBCT

4. non-surgical retreatment unfeasible (post, anatomical complexity, iatrogenic errors) or previously failed treatment.

5. Good periodontal health condition at tooth level.

6. Able to completely understand and sign an informed consent form.

Exclusion criteria:

1. Presence of vertical root fracture

2. Presence of root perforations

3. Miller class III/IV mobility

4. Presence of root resorption

5. Combined endodontic-periodontic lesions.

6. Pregnancy

Related Conditions & MeSH terms

• Blood Loss, Surgical
• Hemorrhage
• Periapical Lesion

Intervention

Procedure:
• conventional surgery
Surgery performed using conventional rotary burs
• piezoelectric device
surgery performed using piezoelectric device.

Locations

Country	Name	City	State
India	PGIDS	Rohtak	Haryana

Sponsors (1)

Lead Sponsor	Collaborator
Postgraduate Institute of Dental Sciences Rohtak

Country where clinical trial is conducted

India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quality of life assessment	to assess pain, swelling, mouth opening and effect on daily activities of patient among piezosurgery and conventional surgery using patient perception questionnaire; aon, swelling, mouth opening and any effect on	till 7 days after surgery
Primary	hemorrhage control	to assess intraoperative hemorrhage control among 2 groups	During surgery
Secondary	periapical healing	periapical healing comparison in 2 groups 2D radiographic healing by Rud et al and Molven et al criteria and 3D healing by modified PENN 3D criteria	Base line to 12 months