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Autogenous Ramus Bone Block Harvesting With Piezosurgery

Primary Purpose

Alveolar Bone Resorption

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Bone harvesting from ramus area with piezosurgery for autogenous bone augmentation
Bone harvesting from ramus area with conventional burs for autogenous bone augmentation
Sponsored by
Marmara University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alveolar Bone Resorption

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • ASA I-II
  • The main inclusion criteria were severe alveolar ridge atrophy in the horizontal plane (≤4 mm) and no accompanying vertical defect, according to preoperative CBCT scans.

Exclusion Criteria:

  • Individuals who had systemic disease affecting bone or soft tissue metabolism
  • Smokers (more than 10 cigarettes a day
  • Alcohol dependent
  • Systemic disease affecting bone or soft tissue metabolism
  • Donor field in the mouth of another region (simfiz, tuber etc.) or any extra-oral field is planned to be used
  • Patients with cleft lip-palate or defect exceeding the alveolar crest
  • Grafts applied to defects caused by tumors, osteoradionecrosis, or congenital malformations
  • Patients with an unstable systemic condition such as metabolic bone disease, uncontrolled diabetes, or untreated hypothyroidism, as well as smokers, patients undergoing radiation therapy or chemotherapy

Sites / Locations

  • Marmara University School of Dentistry

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Piezosurgery Group

Conventional Group

Arm Description

In the experimental group, a piezosurgical device was used to harvest the bone block from the ramus area.

In the experimental group, a conventional burr was used to harvest the bone block from the ramus area.

Outcomes

Primary Outcome Measures

Osteotomy time
The time from the start of the osteotomy to the luxation of the bone block was measured with the help of a digital stopwatch.

Secondary Outcome Measures

Change in pain
Postoperative pain was assessed using a Visual Analogue Scale (VAS) ranging from the absence of pain (score 0) to the most severe pain imaginable
Change in Mouth opening
The distance between the mesio-incisal corners of the upper and lower central incisors was measured with the help of a ruler when the mouth opening was at its maximum.
Change in Oral Health-related Quality of Life
Evaluated by OHIP-14
Operation time
The total time from the first incision of the operation site to the last suture was measured with the help of a digital stopwatch as the operation time.
Change in facial swelling
With the technique described by Neupert ; Angle of mandible-tragus Angle of mandible-lateral canthus of eye Mandible corner-nose wing Angle of mandible oral-commissures Measurements were made with a tape measure from 5 points, with the mandible corner-pogonion.

Full Information

First Posted
September 14, 2022
Last Updated
September 17, 2022
Sponsor
Marmara University
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1. Study Identification

Unique Protocol Identification Number
NCT05548049
Brief Title
Autogenous Ramus Bone Block Harvesting With Piezosurgery
Official Title
A Prospective Randomized Trial Comparing Conventional And Piezosurgery Method In Mandibular Bone Block Harvesting From The Retromolar Region
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Completed
Study Start Date
September 1, 2021 (Actual)
Primary Completion Date
March 1, 2022 (Actual)
Study Completion Date
July 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Marmara University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this randomized prospective clinical trial was to evaluate the outcome of bone block harvesting from the retromolar region using the Conventional and Piezosurgery Method. The study was planned on 19 patients (13F,6M) on 31 donor sites. In patients with bilateral bone harvesting, the donor site and the surgical method to be used were determined by the randomization protocol, while in patients with bone harvesting from a single site, the donor site was determined by considering parameters such as proximity to the operation site and distance to the inferior alveolar nerve. Clinical parameters such as operation time, pain, swelling, trismus, nerve damage were evaluated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alveolar Bone Resorption

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Piezosurgery Group
Arm Type
Experimental
Arm Description
In the experimental group, a piezosurgical device was used to harvest the bone block from the ramus area.
Arm Title
Conventional Group
Arm Type
Active Comparator
Arm Description
In the experimental group, a conventional burr was used to harvest the bone block from the ramus area.
Intervention Type
Device
Intervention Name(s)
Bone harvesting from ramus area with piezosurgery for autogenous bone augmentation
Intervention Description
In this invervention, the piezo-surgical device settings were set to irrigation: '4', function: 'cortical', light: 'auto'. After the full-thickness flap was lifted with the periosteal elevator, superior and vertical osteotomies were performed with the OT-12 piezo-surgical tip. Lower horizontal osteotomies were performed using OT8-L or OT-8-R piezo tips according to the studied quadrant, combining the vertical osteotomy.
Intervention Type
Device
Intervention Name(s)
Bone harvesting from ramus area with conventional burs for autogenous bone augmentation
Intervention Description
In control group, After the full-thickness flap is lifted with the periosteal elevator, using a thin #9 fissure burand the surgical handpiece S-11 Straight tip , the physiodispenser settings are according to the manufacturer's recommendations. The osteotomy was performed after it was adjusted to 40,000 rpm as appropriate. Bone incisions were completed with a round bur to combine the lower horizontal osteotomies and 2 vertical osteotomies. The osteotomies were completed with the help of a thin flat drill, and the block graft was carefully separated from the donor site.
Primary Outcome Measure Information:
Title
Osteotomy time
Description
The time from the start of the osteotomy to the luxation of the bone block was measured with the help of a digital stopwatch.
Time Frame
Intraoperative
Secondary Outcome Measure Information:
Title
Change in pain
Description
Postoperative pain was assessed using a Visual Analogue Scale (VAS) ranging from the absence of pain (score 0) to the most severe pain imaginable
Time Frame
7 days
Title
Change in Mouth opening
Description
The distance between the mesio-incisal corners of the upper and lower central incisors was measured with the help of a ruler when the mouth opening was at its maximum.
Time Frame
7 days
Title
Change in Oral Health-related Quality of Life
Description
Evaluated by OHIP-14
Time Frame
14 days
Title
Operation time
Description
The total time from the first incision of the operation site to the last suture was measured with the help of a digital stopwatch as the operation time.
Time Frame
Intraoperative
Title
Change in facial swelling
Description
With the technique described by Neupert ; Angle of mandible-tragus Angle of mandible-lateral canthus of eye Mandible corner-nose wing Angle of mandible oral-commissures Measurements were made with a tape measure from 5 points, with the mandible corner-pogonion.
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: ASA I-II The main inclusion criteria were severe alveolar ridge atrophy in the horizontal plane (≤4 mm) and no accompanying vertical defect, according to preoperative CBCT scans. Exclusion Criteria: Individuals who had systemic disease affecting bone or soft tissue metabolism Smokers (more than 10 cigarettes a day Alcohol dependent Systemic disease affecting bone or soft tissue metabolism Donor field in the mouth of another region (simfiz, tuber etc.) or any extra-oral field is planned to be used Patients with cleft lip-palate or defect exceeding the alveolar crest Grafts applied to defects caused by tumors, osteoradionecrosis, or congenital malformations Patients with an unstable systemic condition such as metabolic bone disease, uncontrolled diabetes, or untreated hypothyroidism, as well as smokers, patients undergoing radiation therapy or chemotherapy
Facility Information:
Facility Name
Marmara University School of Dentistry
City
Istanbul
ZIP/Postal Code
34854
Country
Turkey

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
Data will become available in 1 month and will be available for 2 years
Citations:
PubMed Identifier
17172961
Citation
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Results Reference
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17514884
Citation
Sohn DS, Ahn MR, Lee WH, Yeo DS, Lim SY. Piezoelectric osteotomy for intraoral harvesting of bone blocks. Int J Periodontics Restorative Dent. 2007 Apr;27(2):127-31.
Results Reference
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17112705
Citation
Robiony M, Polini F, Costa F, Zerman N, Politi M. Ultrasonic bone cutting for surgically assisted rapid maxillary expansion (SARME) under local anaesthesia. Int J Oral Maxillofac Surg. 2007 Mar;36(3):267-9. doi: 10.1016/j.ijom.2006.08.013. Epub 2006 Nov 16.
Results Reference
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PubMed Identifier
29534125
Citation
Hanser T, Doliveux R. MicroSaw and Piezosurgery in Harvesting Mandibular Bone Blocks from the Retromolar Region: A Randomized Split-Mouth Prospective Clinical Trial. Int J Oral Maxillofac Implants. 2018 Mar/Apr;33(2):365-372. doi: 10.11607/jomi.4416.
Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
31094060
Citation
Pereira RS, Pavelski MD, Griza GL, Boos FBJD, Hochuli-Vieira E. Prospective evaluation of morbidity in patients who underwent autogenous bone-graft harvesting from the mandibular symphysis and retromolar regions. Clin Implant Dent Relat Res. 2019 Aug;21(4):753-757. doi: 10.1111/cid.12789. Epub 2019 May 16.
Results Reference
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PubMed Identifier
19885448
Citation
Chiapasco M, Casentini P, Zaniboni M. Bone augmentation procedures in implant dentistry. Int J Oral Maxillofac Implants. 2009;24 Suppl:237-59.
Results Reference
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PubMed Identifier
33262880
Citation
Starch-Jensen T, Deluiz D, Deb S, Bruun NH, Tinoco EMB. Harvesting of Autogenous Bone Graft from the Ascending Mandibular Ramus Compared with the Chin Region: a Systematic Review and Meta-Analysis Focusing on Complications and Donor Site Morbidity. J Oral Maxillofac Res. 2020 Nov 30;11(3):e1. doi: 10.5037/jomr.2020.11301. eCollection 2020 Jul-Sep.
Results Reference
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Citation
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Results Reference
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32480048
Citation
Nielsen HB, Starch-Jensen T. Lateral ridge augmentation in the posterior part of the mandible with an autogenous bone block graft harvested from the ascending mandibular ramus. A 10-year retrospective study. J Stomatol Oral Maxillofac Surg. 2021 Apr;122(2):141-146. doi: 10.1016/j.jormas.2020.05.020. Epub 2020 May 29.
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Autogenous Ramus Bone Block Harvesting With Piezosurgery

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