The Effect of Different Antibiotic Protocols on Peri-implant Tissue Health

NCT ID: NCT06378502

Last Updated: 2024-04-22

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE4
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-05-03
• Study Completion Date: 2026-06-30

Brief Summary

The aim of the present project (non-inferiority trial) is to evaluate the effect of different antibiotic strategies (long-span vs. short-span) for implant surgery on peri-implant tissue health, oral microbiome (included resistome) and salivary MiRNomics in healthy patients.

Detailed Description

A total of 80 patients will be included and randomly divided in two groups:

1. Long-span prescription: 1 g Amoxicillin every 8 h starting 1 day before surgery and for 5 days after surgery

2. Short-span prescription: 2 g Amoxicillin 1 h before surgery Before surgery, patients will undergo an antibiotic sensitivity test (AST), and non-invasive samples will be taken to analyse oral microbiome including resistome. Saliva samples will be also taken for miRNomics analysis. Patients will be rehabilitated with single implants or partial implant-supported fixed prostheses. The day of surgery, samples of peripheral blood will be taken and peripheral blood mononuclear cells (PBMCs) isolated from the first 30 patients in order to implement a micro-fluidic bioreactor replicating the bone healing process of each patient. 3D bone models will be developed that are suitable for drug screening.

At 2 and 6 months post-treatment, AST test and oral microbiome and resistome analysis will be performed again. 2 months after treatment, a new saliva sample of the patients will be also taken, analysed and compared using MiRnomics technology with the preoperative one with the further aim of identifying reliable biomarkers of mucositis and perimplantitis. During the 12-month follow-up implant survival rate, marginal bone loss (MBL), biologic and technical complication rate and peri-implant health parameters (including plaque index, probing depth and bleeding on probing) will be evaluated.

Parametric or non-parametric comparative tests, as appropriate, will be performed to detect differences between the groups in the various outcome variables. The effect of patient-related and implant-related predictive factors on the various outcomes will be evaluated using multilevel logistic regression analysis. Metadata will be analyzed also with 4th generation Artificial Neural Networks (ANNs) (machine learning) using unsupervised and supervised systems.

Expected results: The present project is expected to clarify if the short-span antibiotic therapy is not inferior to the long-span one in healthy patients undergoing implant surgery. The outcomes will contribute to the development of effective clinical guidelines that will help to tackle the issue of antimicrobial resistance. In addition, the development and validation of a 3D bone model to be used for drug screening is expected, that might overcome limitations of currently available 2D bone models and animal studies. A further expected result is the identification of biomarkers for diagnosis and prognosis in implant dentistry, through salivary miRNomics that might lead to the development of a non-invasive liquid biopsy.

Conditions

Antibiotic

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Long-span therapy

1 g Amoxicillin every 8 h starting 1 day before surgery and for 5 days after surgery

Group Type: EXPERIMENTAL

Amoxicillin Long

Intervention Type: DRUG

Long span

Short-span therapy

2 g Amoxicillin 1 h before surgery

Group Type: EXPERIMENTAL

Amoxicillin Short

Intervention Type: DRUG

Short Span

Interventions

Amoxicillin Short

Short Span

Intervention Type: DRUG

Amoxicillin Long

Long span

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

Healthy volunteers requiring one single implant or partial implant-supported rehabilitation in an edentulous area of the posterior mandible or maxilla

Exclusion Criteria

• Patients unable to commit to follow-up
• General contraindications to implant surgery
• Immuno-suppressed/immune-compromised patients
• Patients irradiated in the head and/or neck
• Uncontrolled diabetes
• Pregnancy, childbearing potential, breastfeeding
• Smoking habit
• Untreated periodontal disease (Caton et al, J Clin Periodontol 2018)
• Poor oral hygiene and motivation (plaque index > 20%)
• Addiction to alcohol or drugs
• Psychiatric problems and/or unrealistic expectations
• Patients with an acute infection (abscess) or suppuration in the site intended for implant placement
• Patients treated or under treatment with intravenous amino-bisphosphonates
• Patients referred only for implant placement if the follow-up cannot be done at the treatment center
• Patients participating in other studies, if the present protocol could not be fully adhered to
• Patients with allergy/hypersensitivity to penicillin or drug excipients
• Patients recently treated with antibiotics for other indications

• Minimum Eligible Age: 35 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Universita degli Studi di Genova

OTHER

Sponsor Role: lead

Responsible Party

Maria Menini

Prof

Responsibility Role: PRINCIPAL_INVESTIGATOR

Central Contacts

Maria Menini

Role: CONTACT

maria.menini@unige.it

3396598789‬

Other Identifiers

antibiotic-resistence

Identifier Type: -

Identifier Source: org_study_id