Catholic University
Roma, 00168, Italy
Location contact
Carlo Lajolo, MD, DDS, PhD
CONTACT
3356078354 ext. +39
Carlo Lajolo, MD,DDS,PhD
PRINCIPAL_INVESTIGATOR
Gioele Gioco, DDS
CONTACT
3288486585 ext. +39
Gioele Gioco, DDS
SUB_INVESTIGATOR
NCT Number: NCT06622421
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
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
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Roma, 00168, Italy
Carlo Lajolo, MD, DDS, PhD
CONTACT
3356078354 ext. +39
Carlo Lajolo, MD,DDS,PhD
PRINCIPAL_INVESTIGATOR
Gioele Gioco, DDS
CONTACT
3288486585 ext. +39
Gioele Gioco, DDS
SUB_INVESTIGATOR
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):
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:
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
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
Time frame: 12 months
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).
Time frame: at the end of surgery
Assessment of operators discomfort during surgery by submitting a questionnaire at the end of surgery
Time frame: during the surgery
Assessment of the ambient noise level during the intervention with a Decibel detector (Protmex PT6708)
Time frame: during the surgery
Evaluation of the duration of the surgery (Chronometer) of the osteotomy
Time frame: 8 hours after surgery and then at 7 and 21 days after surgery
Assess whether there is a correlation between clinical parameters of healing (modified Landry's Healing Index) and patient's subjective perception
Time frame: 8 hours after surgery and then at 7 and 21 days after surgery
Identify any risk factors associated with unfavorable postoperative course both in terms of clinical healing and subjective perception
Time frame: 8 hours after surgery and then at 7 and 21 days after surgery
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.
Time frame: 8 hours after surgery and then at 7 and 21 days after surgery
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.
Time frame: 8 hours after surgery and then at 7 and 21 days after surgery
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.
Time frame: after surgery at 7 and 21 days after surgery
Assessment of clinical healing of sites undergoing marginal resective surgery using the modified Landry Healing Index
Contact information is provided by the study sponsor or research team.
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Other
Piezoeletric Surgery vs Conventional Surgery for Treatment of Medication-related Osteonecrosis of the Jaws: a Randomized Clinical Trial
Acronym: PIEZOPZ-1
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.
Published trials that share one or more normalized conditions with this study.
NCT06457776
Bisphosphonate-Associated Osteonecrosis, Bisphosphonate-Associated Osteonecrosis of the Jaw
Roma, Italy
View Trial DetailsNCT01325142
Bisphosphonate-Associated Osteonecrosis of the Jaw, Bone Diseases
Ann Arbor, Michigan, United States
View Trial DetailsNCT07588269
Medication-related Osteonecrosis of the Jaw, Osteonecrosis of the Jaw
View Trial DetailsNCT06419010
Osteonecrosis of the Jaw
Bordeaux, France
View Trial Details