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Bisphosphonate-Associated Osteonecrosis of the JawPIEZOPZ-1NCT06622421

Piezoeletric Surgery vs Conventional Surgery for Treatment of MRONJ

A study testing Piezoelectric surgery and Conventional surgery in people with Bisphosphonate-Associated Osteonecrosis of the Jaw and Osteonecrosis of the Jaw, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS at 1 site in Italy.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

To date, surgical therapy of MRONJ remains the therapy of choice while still in association with a medical approach. Surgical intervention aims to stop the progression of the pathology through the removal of the tissue macroscopically affected (resective surgery,sequestrectomy, debridement). Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Piezoelectric surgery and Conventional surgery
Could I receive a placebo?
No, everyone receives an active treatment
How many people
34 participants
Where
1 siteItaly
Study dates
1 Dec 2025to 1 Sep 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Ability to understand the information provided and to give free consent;
  • Age greater than 18 years at the time of diagnosis;
  • Diagnosis of stage 1 or stage 2 MRONJ, according to the SICMF-SIPMO classification [1];
  • Need for surgical treatment of MRONJ.

Who cannot join

  • Patients with a previous history of radiotherapy in the head and neck area;
  • Patients with psychiatric disorders;
  • Women of childbearing age
  • Patients in stages of MRONJ other than stage 1 and 2;
  • Patients undergoing retreatment of MRONJ;
  • Patients with general medical contraindications for oral surgery procedures;
  • Patients unable to attend the outpatient visits required by the protocol.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Carlo Lajolo, MD,DDS, PhD contact

3356078354 ext. +39

carlo.lajolo@unicatt.it

Italy1 site
  • Catholic University

    Roma, 00168

    Carlo Lajolo, MD, DDS, PhD, 3356078354 ext. +39, carlo.lajolo@unicatt.it

    Gioele Gioco, DDS, 3288486585 ext. +39, gioele.gioco@unicatt.it

Other trials in Italy

About this study

Official title: Piezoeletric Surgery vs Conventional Surgery for Treatment of Medication-related Osteonecrosis of the Jaws: a Randomized Clinical Trial

To date, surgical therapy of MRONJ remains the therapy of choice while still in association with a medical approach. Surgical intervention aims to stop the progression of the pathology through the removal of the tissue macroscopically affected (resective surgery,sequestrectomy, debridement).

These surgical procedures are classically performed by the use of handpiece burs, but due to the advent of piezoelectric surgery in dentistry, a comparison of the two techniques is required

Read more

At present there are no randomized clinical trials designed to compare the postoperative discomfort of the two previously described techniques in the treatment of MRONJ. Therefore, the aim of this study is to evaluate the postoperative discomfort in a group of patients undergoing surgical therapy for MRONJ with piezoelectric instruments compared to a control group undergoing MRONJ surgical therapy with traditional rotary instruments.

METHODS This is a randomized clinical trial conducted in patients diagnosed with MRONJ who require surgical therapy.

Patients will be recruited and evaluated for a period of 24 months. Follow-up of patients enrolled in the study will last 12 months. Specifically, once patients diagnosed with MRONJ requiring surgical therapy are identified, surgery will be scheduled within 1 month, then follow-up visits will be conducted at 1, 2, 3 weeks and 3, 6, 12 months after surgery.

Patients enrolled and randomized into one of the two groups will all undergo necrotic bone removal surgery by the same operator with decades of experience in treating MRONJs. Marginal bone resection surgery will be performed using rotary or piezoelectric instruments. Both surgical procedures involve wound closure by first intention healing using sutures. Each bone block removed will undergo histologic examination for diagnostic confirmation of osteonecrosis. Postoperative instructions will be explained to patients, and sutures will be removed at 7 or 14 days after surgery.

Each patient will be asked for a 3D radiologic exam (CT or CBCT) at least 12 months after surgery in order to asses the

Read the detailed description

Medicaiton-related osteonecrosis of the jaw (MRONJ) is defined as a drug-related adverse reaction characterized by progressive destruction and necrosis of the mandibular and/or maxillary bone in subjects exposed to treatment with drugs known to be at increased risk of disease, in the absence of previous radiation treatment. The first case of osteonecrosis was described in 2003 by Marx et al. in association with a specific group of drugs used in the treatment of skeletal system diseases: bisphosphonates, in particular the category of amino-bisphosphonates (i.e., zoledronate, pamidronate, alendronate) has been linked to the onset of MRONJ. However, from 2008, the first reports of MRONJ in association with other categories of drugs appeared: denosumab and targeted therapy as cancer treatment, such as bevacizumab, sunitinib, everolimus, etc. Bisphosphonates and denosumab are drugs used to treat osteometabolic (e.g. osteoporosis), oncological (e.g. bone metastases from solid tumors) and hematological diseases, available on the market in the form of oral or parenteral formulations (intravenous, intramuscular, subcutaneous). These drugs determine, through different mechanisms, an inhibition of osteoclastic activity and, consequently, an alteration of bone turnover. Target therapy are instead used only in the treatment of oncological diseases and mostly have an anti-angiogenic activity. The risk of onset of MRONJ varies mainly based on the type of drug administered, the administration route and the type of disease for which the intake was necessary; in particular, it has emerged that the risk is increased in case of intravenous administration and a higher cumulative dose, which is why cancer patients would seem to have a higher risk of developing MRONJ compared to subjects who use anti-resorbable drugs for osteo-metabolic diseases. The diagnostic process is complex and requires the integration of different clinical and radiological signs. In the past, the key element for the diagnosis of MRONJ was the presence of exposed necrotic bone inside the oral cavity, however in the literature it has emerged that a significant number of patients treated with these drugs present signs and symptoms, both in the initial and late phase, different from bone exposure alone. The diagnosis of MRONJ is structured according to the diagnostic work-up proposed by SICMF (Italian Society of Maxillo-Facial Surgery) - SIPMO (Italian Society of Oral Pathology and Medicine):

  • Step 1: diagnostic suspicion deriving from the medical, dental and pharmacological history
  • Step 2: differential diagnosis through identification of clinical signs (bad breath, odontogenic abscess, mandibular asymmetry, pain of dental and/or bone origin, exposure of necrotic bone, mucosal fistula, extra-oral fistula, hyperemia of the mucosa, failure to repair the alveolar mucosa after extraction, rapid onset of tooth mobility, preternatural mobility of the mandible, with or without preserved occlusion, paresthesia/dysesthesia of the lips, discharge from the nose, purulent discharge, spontaneous sequestration of bone fragments, trismus, swelling of the soft tissues), evaluation of pain and 1st level imaging (orthopantomography and/or intraoral radiography);
  • Step 3: conclusive diagnosis through 2nd level imaging (CT Dentascan or Cone-Beam) These new diagnostic elements have allowed us to frame the pathology within a staging based on minor clinical signs and radiological signs. Reference is made to the staging proposed by SICMF - SIPMO. The importance of a correct diagnosis and therefore the inclusion of the pathology within a given stage lies in the variability and invasiveness of the therapeutic approach to MRONJ.

The treatment of MRONJ includes the possibility of medical and/or surgical therapy, although there is still no worldwide guidelines.

Medical therapy involves the use of drugs aimed at controlling the infection with the aim of stabilizing the clinical features by slowing the progression of the disease, but it is a very conservative approach that is unlikely to determine a complete resolution of the pathology. It consists of the association of an antiseptic therapy with chlorhexidine-based mouthwashes for disinfecting the oral cavity and an antibiotic therapy based on penicillins or in allergic patients quinolones, metronidazole, clindamycin and doxycycline.

Surgical therapy of MRONJ, however, remains the therapy of choice to date, although always in association with a medical approach. The surgical intervention, in fact, aims to stop the progression of the pathology through the removal of the tissue macroscopically involved in the disease until healthy bone tissue is reached.

The invasiveness of surgical techniques is strictly related to the staging and extension of MRONJ and, although there are no standard protocols, the aforementioned techniques can empirically be divided into:

  • Resective surgery which involves the en bloc removal of the pathological bone until reaching the healthy vital tissue. It can be divided into segmental or marginal resective surgery if the intervention involves or does not involve the interruption of the anatomical continuity of the affected skeletal segment.
  • Sequestrectomy which allows the surgical removal of a bone sequestration in the maxillary and/or mandibular area and is a simpler therapy than resective surgery, although there is difficulty in precisely identifying the microscopic limit between the bone involved in the disease and healthy tissue.
  • Debridement which involves the surgical removal of necrotic bone tissue until a bleeding bone surface is identified. This procedure requires that the necrotic bone is not yet separated from the surrounding vital bone, otherwise it would be a sequestrectomy.

These surgical procedures are classically performed using burs mounted on a straight handpiece, but the advent of piezoelectric surgery in various areas of oral surgery has led us to the need for a comparison between the two techniques in the field of surgical treatment of MRONJ.

In the last 20 years, the use of ultrasonic vibrations has become routine for standard clinical applications in many fields of surgery, as it is able to reduce the risk of damage to the surrounding soft tissues and critical structures such as vessels and nerves during the osteotomy. Piezosurgery, in fact, would allow greater precision in cutting, protection of vascular-nervous structures and better visibility of the surgical field, compared to rotating instruments. These properties are determined by the fact that frequencies between 25-29 kHz are used, capable of determining a selective cut of mineralized tissues compared to soft tissues. According to some studies, moreover, piezoelectric bone surgery seems to be more efficient in the first phase of bone healing, inducing an early colonization of the residual bone by bone morphogenetic proteins, a greater control of inflammation and therefore a faster bone remodeling. Some authors have attributed the following limitations to this technique: prolonged operating time, learning difficulties and the risk of determining bone overheating in the case of excessive working pressure [9]. Consequently, there is no agreement, considering the available evidence, on which surgical technique represents the gold standard in the treatment of MRONJ, especially in reference to the perception of post-operative discomfort by the patient.

At present, to the best of the authors\' knowledge, there are no randomized clinical studies aimed at comparing the post-operative discomfort of the two techniques previously described, in the treatment of MRONJ.

AIM The primary objective of this randomized controlled trial (RCT) is to evaluate postoperative pain and discomfort in a group of patients undergoing surgical therapy for MRONJ with piezoelectric instruments, using as a control a group of patients undergoing surgical therapy for MRONJ with traditional rotary instruments. Secondary objectives will focus on the evaluation of clinical healing of the site, operator discomfort, discomfort felt by the patient during the procedure, duration of the procedure and the occurrence of disease recurrence over the following 12 months. An additional objective of the study is the preoperative definition of a radiographic margin of bone resection associated with a lower rate of MRONJ recurrence by comparing the preoperative and postoperative three-dimensional radiographic examination (12 months after surgery).

Study design This is a prospective randomized and controlled parallel-group (1:1) superiority study. The study will be conducted blindly for the operator who collects the data and for the statistician, in order to ensure greater validity of the results. Randomization will occur after the flap lifting, preparatory to the surgical intervention of marginal resective surgery for the treatment of MRONJ. A randomization envelope will be opened at that moment, and the operator (the same for all the surgical procedures being studied) will proceed to complete the therapy with one or the other technique.

Study setting The study will be carried out at the UOC of General Dentistry and Orthodontics of the Fondazione Policlinico A. Gemelli - IRCSS. The care setting in which the patients enrolled in this study will be treated is of an outpatient type.

Being tested
Piezoelectric surgery, Conventional surgery
Keywords
MEDICATION RELATED OSTEONECROSIS OF THE JAW, SURGICAL TREATMENT OF MRONJ, MRONJ
Medical subject headings
Bisphosphonate-Associated Osteonecrosis of the Jaw

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Piezoelectric surgeryDevice

    Patients enrolled and randomized into one of the two groups will all undergo surgery to remove necrotic bone on an outpatient basis by the same operator with a decade of experience in the treatment of MRONJ. As per clinical routine, a marginal bone resection procedure will be performed using rotary instruments or piezoelectric instruments (depending on the assignment to one of the two groups). Both surgical procedures involve complete closure of the wound by primary intention using sutures

  • Conventional surgeryProcedure or surgery

    Patients enrolled and randomized into one of the two groups will all undergo surgery to remove necrotic bone on an outpatient basis by the same operator with a decade of experience in the treatment of MRONJ. As per clinical routine, a marginal bone resection procedure will be performed using rotary instruments or piezoelectric instruments (depending on the assignment to one of the two groups). Both surgical procedures involve complete closure of the wound by primary intention using sutures

Study groups in NCT06622421
Study groupRoleWhat they receive
G1 - control groupOtherPatients with MRONJ diagnosis who will undergo to conventional surgery using rotary burns instruments
Receives: Procedure: Conventional surgery
G2 - study groupExperimentalPatients with MRONJ diagnosed who will undergo to piezoelectric surgery
Receives: Device: Piezoelectric surgery

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. MRONJ healing

    Evaluation of disease recurrence over the following 12 months: this evaluation will be performed clinically (absence of symptoms, absence of exposed bone in the oral cavity, and other minor clinical signs) and radiographically through a routinely required 3D radiographic exam (CBCT or CT).

    Measured: 12 months

Secondary outcomes (9)
  1. operators discomfort

    Assessment of operators discomfort during surgery by submitting a questionnaire at the end of surgery

    Measured: at the end of surgery

  2. ambient noise

    Assessment of the ambient noise level during the intervention with a Decibel detector (Protmex PT6708)

    Measured: during the surgery

  3. duration of the surgery

    Evaluation of the duration of the surgery (Chronometer) of the osteotomy

    Measured: during the surgery

  4. correlation between clinical parameters and patient's perception

    Assess whether there is a correlation between clinical parameters of healing (modified Landry\'s Healing Index) and patient\'s subjective perception

    Measured: 8 hours after surgery and then at 7 and 21 days after surgery

  5. Risk factors

    Identify any risk factors associated with unfavorable postoperative course both in terms of clinical healing and subjective perception

    Measured: 8 hours after surgery and then at 7 and 21 days after surgery

  6. postoperative discomfort OHIP

    Assessment of postoperative discomfort of patients undergoing marginal resective surgery (OHIP-14). These questionnaires will be administered at 8 hours after surgery and then at 7 and 21 days after surgery.

    Measured: 8 hours after surgery and then at 7 and 21 days after surgery

  7. postoperative discomfort - QoR

    Assessment of postoperative discomfort of patients undergoing marginal resective surgery (QoR-15). These questionnaires will be administered at 8 hours after surgery and then at 7 and 21 days after surgery.

    Measured: 8 hours after surgery and then at 7 and 21 days after surgery

  8. postoperative discomfort (NRS)

    Assessment of postoperative pain (NRS-10). These questionnaires will be administered at 8 hours after surgery and then at 7 and 21 days after surgery.

    Measured: 8 hours after surgery and then at 7 and 21 days after surgery

  9. Clinical Healing HI

    Assessment of clinical healing of sites undergoing marginal resective surgery using the modified Landry Healing Index

    Measured: after surgery at 7 and 21 days after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Oct 2024
  2. Study start1 Dec 2025 (estimated)
  3. Primary completion1 Sep 2026 (estimated)
  4. Study completion1 Sep 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a prospective randomized and controlled study with parallel groups (1:1) of superiority
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
34 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06622421
Sponsor's protocol ID
5786
Acronym
PIEZOPZ-1
Status last verified
Sep 2024
First submitted
16 Jul 2024
Last updated
22 Sep 2025
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Marx RE. Pamidronate (Aredia) and zoledronate (Zometa) induced avascular necrosis of the jaws: a growing epidemic. J Oral Maxillofac Surg. 2003 Sep;61(9):1115-7. doi: 10.1016/s0278-2391(03)00720-1. No abstract available.

    PubMed 12966493
  • Mavrokokki T, Cheng A, Stein B, Goss A. Nature and frequency of bisphosphonate-associated osteonecrosis of the jaws in Australia. J Oral Maxillofac Surg. 2007 Mar;65(3):415-23. doi: 10.1016/j.joms.2006.10.061.

    PubMed 17307586
  • Yarom N, Fedele S, Lazarovici TS, Elad S. Is exposure of the jawbone mandatory for establishing the diagnosis of bisphosphonate-related osteonecrosis of the jaw? J Oral Maxillofac Surg. 2010 Mar;68(3):705. doi: 10.1016/j.joms.2009.07.086. No abstract available.

    PubMed 20171493
  • Ruggiero SL, Dodson TB, Fantasia J, Goodday R, Aghaloo T, Mehrotra B, O'Ryan F; American Association of Oral and Maxillofacial Surgeons. American Association of Oral and Maxillofacial Surgeons position paper on medication-related osteonecrosis of the jaw--2014 update. J Oral Maxillofac Surg. 2014 Oct;72(10):1938-56. doi: 10.1016/j.joms.2014.04.031. Epub 2014 May 5.

    PubMed 25234529
  • Colella G, Campisi G, Fusco V. American Association of Oral and Maxillofacial Surgeons position paper: Bisphosphonate-Related Osteonecrosis of the Jaws-2009 update: the need to refine the BRONJ definition. J Oral Maxillofac Surg. 2009 Dec;67(12):2698-9. doi: 10.1016/j.joms.2009.07.097. No abstract available.

    PubMed 19925998
  • El-Rabbany M, Sgro A, Lam DK, Shah PS, Azarpazhooh A. Effectiveness of treatments for medication-related osteonecrosis of the jaw: A systematic review and meta-analysis. J Am Dent Assoc. 2017 Aug;148(8):584-594.e2. doi: 10.1016/j.adaj.2017.04.002. Epub 2017 May 18.

    PubMed 28527518
  • Labanca M, Azzola F, Vinci R, Rodella LF. Piezoelectric surgery: twenty years of use. Br J Oral Maxillofac Surg. 2008 Jun;46(4):265-9. doi: 10.1016/j.bjoms.2007.12.007. Epub 2008 Mar 14.

    PubMed 18342999

Questions about this trial

What is this clinical trial studying?

A study testing Piezoelectric surgery and Conventional surgery in people with Bisphosphonate-Associated Osteonecrosis of the Jaw and Osteonecrosis of the Jaw, run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 22 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Carlo Lajolo, MD,DDS, PhD (3356078354 ext. +39, carlo.lajolo@unicatt.it), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

MRONJ healing (time frame: 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06622421, which also lists 7 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Sep 2025.

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