Experimental Peri-implant Mucositis on Implant Sites That Were Previously Treated With or Without Implantoplasty

NCT ID: NCT06063876

Last Updated: 2025-10-10

Basic Information

• Recruitment Status: ENROLLING_BY_INVITATION
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-09-05
• Study Completion Date: 2026-06-30

Brief Summary

This controlled clinical trial will assess clinically, immunologically, and microbiologically the healing of experimental peri-implant mucositis (PIM) lesions in implants treated previously with implantoplasty (IP) compared to those treated without IP.

Detailed Description

The present parallel controlled clinical trial is designed as a 21-day experimental peri-implant mucositis, followed by a period of resolution of 21 days in healthy implants that were previously treated for peri-implantitis with and without implantoplasty.

A total of 8 appointments over the course of about 42 days will be necessary. These appointments will take place in the Department of Periodontics & Preventive Dentistry and are described as follows:

Screening Appointment (14 days prior to Day 0): During this visit, informed consent will be obtained from each subject and inclusion criteria for participation in the study will be reviewed. Participants will undergo the following activities:

• Review of medical, dental history and medications
• Periodontal chart
• Intraoral photographs
• Periapical radiograph of the dental implant that was previously treated with or without implantoplasty to confirm if the implant is in healthy condition with no progressive bone loss
• A digital impression (intraoral scan) of the teeth will be taken for fabrication of a customized stent (a plastic cover). The participant will be instructed to place the stent over the implant whenever performing oral care measures (brushing/flossing/mouthrinse) at home for 21 days. The authors will teach the individuals on how to use this stent and how to brush the teeth/implant(s) during the study. The stent will be provided at the next research visit.
• A professional prophylaxis (dental cleaning) of all tooth and implant surfaces.

V2 - V5 (from day 0 to day 21), the experimentally induced peri-implant mucositis phase, the participant will be wearing the stent over the implant area during their routine oral health care. The following research activities will occur:

• Review any changes to medical or dental history and any new medications
• Intraoral photographs
• Clinical assessment
• Peri-implant crevicular fluid sample collection from the deepest pocket around the implant using paper points.
• Biofilm sample collection using sterile curettes (titanium or plastic) at the same sites.

At V5 (day 21), the participants will receive a dental cleaning, polishing, and review of their oral hygiene home care techniques. Then, they will be asked to reinstitute their oral hygiene home care procedures.

At V6 - V8 (from day 28 to day 42), the resolution of induced peri-implant mucositis phase, the following research activities will occur:

• Review any changes to medical or dental history and any new medications
• Intraoral photographs
• Clinical assessment
• Peri-implant crevicular fluid sample collection from the deepest pocket around the implant using paper points.
• Biofilm sample collection using sterile curettes (titanium or plastic) at the same sites.

At V8 (day 42), a new periapical radiograph will be acquired. If there is still any evidence of inflammation around the implant, we will continue to monitor/treat the inflammation every 3-4 weeks until it is resolved.

PERI-IMPLANT CREVICULAR FLUID (PICF) SAMPLING AND ANALYSIS:

PICF samples will be collected weekly. The site with the deepest pocket of each implant will be sampled using sterile Periopapers with colored bands (29 mm, ISO 25, taper .02; VDW, Munich, Germany). At each visit following screening (V2-V8), the samples will be taken from the same site. The PICF volume will be measured with a calibrated, electronic gingival fluid measuring device (Periotron 8000, Oraflow, Plainview, NY, USA). Cytokines will be detected using a panel of relevant cytokines using a bead based multiplex immunoassay (Bio-Plex Pro Human Cytokine 27-plex Assay).

SUBMUCOSAL PLAQUE SAMPLING AND DNA EXTRACTION Sterile curettes (titanium or plastic) will be used to collect plaque samples from the deepest pocket around each implant. DNA will be extracted using DNeasy Blood and Tissue Kit (Qiagen). Genomic DNA samples will be profiled with 16S Amplicon Sequencing Service. Microbial composition will be profiled with Centrifuge using bacterial, viral, fungal, and human genome datasets.

Conditions

Peri-implant Mucositis; Peri-Implantitis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Implants with history of peri-implantitis

Implant(s) treated previously for peri-implantitis with or without exposed polished surface, no PD \> 4 mm and \< 50% bone loss.

Group Type: EXPERIMENTAL

Induction of experimental peri-implant mucositis

Intervention Type: PROCEDURE

Patients will refrain from oral hygiene measures at the implant sites for 3 weeks to induce peri-implant mucositis, by using a stent in the included implant during oral hygiene.

Resolution of experimental peri-implant mucositis

Intervention Type: PROCEDURE

Patients will reinstitute oral hygiene measures, receive an oral prophylaxis and oral hygiene instructions and will be evaluated during 3 weeks.

Interventions

Induction of experimental peri-implant mucositis

Patients will refrain from oral hygiene measures at the implant sites for 3 weeks to induce peri-implant mucositis, by using a stent in the included implant during oral hygiene.

Intervention Type: PROCEDURE

Resolution of experimental peri-implant mucositis

Patients will reinstitute oral hygiene measures, receive an oral prophylaxis and oral hygiene instructions and will be evaluated during 3 weeks.

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Aged 18-80 years
• In good general health, (at least ASA 2)
• Previously treated implants must have probing depths (PD) ≤ 4 mm
• Previously treated implants must have <50% bone loss around the implant of interest (assessed radiographically)
• Patients must have been treated previously for peri-implantitis with or without IP, with at least 1 thread or 2 mm of implant surface exposed in the oral cavity.
• Have little to no bacteria on the implant(s) of interest (modified Plaque Index of <1) by Day 0
• Have healthy gums that do not bleed around the implant(s) of choice (modified Gingival index <1) by Day 0
• Have evidence of stable bone levels around the treated implant for > 6 months

Exclusion Criteria

• Active infectious diseases of any kind.
• Medical conditions which require premedication prior to dental treatments/visits.
• Pregnant women or planning to become pregnant (self-reported).
• Patients with congenital or metabolic bone disorders (ie. osteoporosis, vitamin D deficiency, parathyroid disease, etc.)
• Current heavy smokers: Subjects who have smoked more than 1 pack/day within 6 months of study onset (self-reported)
• Subjects with co-morbid conditions (i.e., uncontrolled diabetes, cardiovascular disease, impaired kidney function, heart murmur, rheumatic fever, bleeding disorder, hepatitis, tuberculosis, HIV) that would affect the study outcome or interpretation of study results will be excluded.
• Concomitant medications: Subjects on significant concomitant drug therapy for systemic conditions (i.e., Chronic anti-inflammatory medication, antibiotics, anticoagulants, any medication initiated <3 months prior to the screening visit) will not be included in the study. Occasional short-term use (7-14 days) of analgesics or common cold medication is permitted. Such use of these medications will be reviewed and recorded by the Investigator.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Pittsburgh

OTHER

Sponsor Role: lead

Responsible Party

Andrea Ravida

Assistant professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Andrea Ravida

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

Locations

University of Pittsburgh School of Dental Medicine

Pittsburgh, Pennsylvania, United States

Countries

United States

Other Identifiers

STUDY22060181

Identifier Type: -

Identifier Source: org_study_id