NCT07212855

Brief Summary

Dental implants are widely employed in modern dentistry for the rehabilitation of patients affected by edentulism, whether limited to a single missing tooth, multiple adjacent teeth, or involving complete dental arches. In particular, full-arch rehabilitations provide both functional and aesthetic restoration of completely edentulous arches or of severely compromised dentitions that the preservation of the remaining teeth is no longer clinically feasible. Among the various treatment strategies available, the Columbus Bridge Protocol™ represents an established implant-prosthetic approach for full-arch rehabilitation through the use of implant-supported prostheses with immediate functional loading. The non-surgical management of peri-implant diseases can be performed using a variety of tools, which are considered equivalent in effectiveness when used individually, according to the Guidelines for the Prevention and Treatment of Peri-implant Diseases. These include ultrasonic devices with implant-specific tips, titanium curettes, chitosan brushes, and air-polishing systems using glycine-based powders. These instruments effectively remove biofilm and deposits without compromising the implant surface, unlike stainless steel curettes, which can induce microscopic alterations. Such alterations may facilitate microbial colonization and complicate effective biofilm removal. In particular, for the removal of soft deposits, air-polishing devices with glycine powder have been shown to reduce clinical signs of inflammation in cases of peri-implant mucositis and may enhance the efficacy of non-surgical therapy in peri-implantitis. Furthermore, the use of fine-grain powders such as glycine does not cause surface alterations to the hard tissues of natural teeth or to titanium implant surfaces, nor does it lead to epithelial erosion of the soft tissues. In patients with full-arch implant-supported prostheses, air-polishing devices represent an effective method for professional oral hygiene, including the prosthetic-mucosal interface, without requiring prosthesis removal. Regarding home oral hygiene, the Guidelines for the Prevention and Treatment of Peri-implant Diseases do not provide universally applicable recommendations. Instead, they emphasize the importance of personalized instructions and motivation strategies, tailored to the individual needs of each patient. For patients rehabilitated with full-arch implant-supported prostheses, in addition to compliance, prosthetic design must ensure adequate cleanability. Ideally, designs should avoid the reconstruction of soft tissues, thereby facilitating daily hygiene procedures. The primary home-care tools recommended for these patients include manual or electric toothbrushes, sponge dental floss, and interdental brushes. The use of an angled toothbrush has also been suggested to improve access to difficult areas, such as prosthetic surfaces in direct contact with the mucosa and distal cantilevers.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
76

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2024

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 15, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

October 1, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

October 8, 2025

Completed
Last Updated

May 5, 2026

Status Verified

September 1, 2025

Enrollment Period

9 months

First QC Date

October 1, 2025

Last Update Submit

April 28, 2026

Conditions

Keywords

professional oral hygienedomiciliary oral hygienefull arch fixed prosthesisimplant disease prevention

Outcome Measures

Primary Outcomes (1)

  • Plaque on implant abutment

    Plaque Index was recorded on the implants prior to the implementation of any procedure that could potentially lead to biofilm removal, evaluating six sites per implant. The absence or presence of plaque will be assessed using a periodontal probe. Scores can range from 0 (no tooth surfaces with plaque) to 100 (all tooth surfaces have plaque), where 100 is the worst possible result.

    3 months

Secondary Outcomes (4)

  • Plaque on prosthesis

    3 months

  • Bleeding on probing on implant abutment

    3 months

  • Probing depth on implant abutment

    3 months

  • Keratinized mucosa

    3 months

Study Arms (4)

professional oral hygiene with glycine and domiciliary oral hygiene with angle toothbrush

EXPERIMENTAL

Patients randomized to the Test group for professional oral hygiene underwent professional removal of hard and soft deposits using titanium curettes, spongy interdental floss, and air-polishing with glycine powder. The glycine powder used had a particle size of 25 μm and was applied using a supragingival nozzle positioned 3 mm from the prosthetic restoration, with particular attention given to the areas in direct contact with the mucosa. Patients randomized to the Test group for domiciliary oral hygiene procedures - were motivated and instructed to use an angled-handle toothbrush (Specialist Implant, Curasept S.p.A., Saronno, Italy), in addition to a standard toothbrush and implant floss. The specific design of the angled handle was intended to facilitate access to areas that are difficult to clean. In patients rehabilitated with full-arch implant-supported prostheses, these areas typically include distal cantilevers and surfaces in direct contact with the mucosa.

Procedure: Professional oral hygiene with glycine powderDevice: Domiciliary oral hygiene with angle toothbrush

professional oral hygiene with glycine and domiciliary oral hygiene with standard toothbrush

ACTIVE COMPARATOR

Patients randomized to the Test group for professional oral hygiene underwent professional removal of hard and soft deposits using titanium curettes, spongy interdental floss, and air-polishing with glycine powder. The glycine powder used had a particle size of 25 μm and was applied using a supragingival nozzle positioned 3 mm from the prosthetic restoration, with particular attention given to the areas in direct contact with the mucosa. Patients randomized to the Control group for domiciliary oral hygiene procedures were motivated exclusively to use a standard toothbrush and implant floss.

Procedure: Professional oral hygiene with glycine powder

professional oral hygiene without glycine and domiciliary oral hygiene with angle toothbrush

ACTIVE COMPARATOR

Patients randomized to the Control group for professional oral hygiene underwent professional removal of hard and soft deposits exclusively by means of titanium curettes and spongy interdental floss. Patients randomized to the Test group for domiciliary oral hygiene procedures - were motivated and instructed to use an angled-handle toothbrush (Specialist Implant, Curasept S.p.A., Saronno, Italy), in addition to a standard toothbrush and implant floss. The specific design of the angled handle was intended to facilitate access to areas that are difficult to clean. In patients rehabilitated with full-arch implant-supported prostheses, these areas typically include distal cantilevers and surfaces in direct contact with the mucosa.

Device: Domiciliary oral hygiene with angle toothbrush

professional oral hygiene without glycine and domiciliary oral hygiene with standard toothbrush

NO INTERVENTION

Patients randomized to the Control group for professional oral hygiene underwent professional removal of hard and soft deposits exclusively by means of titanium curettes and spongy interdental floss. Patients randomized to the Control group for domiciliary oral hygiene procedures were motivated exclusively to use a standard toothbrush and implant floss.

Interventions

Professional removal of hard and soft deposits using titanium curettes, spongy interdental floss, and air-polishing with glycine powder. The glycine powder used had a particle size of 25 μm and was applied using a supragingival nozzle positioned 3 mm from the prosthetic restoration, with particular attention given to the areas in direct contact with the mucosa.

professional oral hygiene with glycine and domiciliary oral hygiene with angle toothbrushprofessional oral hygiene with glycine and domiciliary oral hygiene with standard toothbrush

Patients were motivated and instructed to use an angled-handle toothbrush (Specialist Implant, Curasept S.p.A., Saronno, Italy), in addition to a standard toothbrush and implant floss. The specific design of the angled handle was intended to facilitate access to areas that are difficult to clean. In patients rehabilitated with full-arch implant-supported prostheses, these areas typically include distal cantilevers and surfaces in direct contact with the mucosa.

professional oral hygiene with glycine and domiciliary oral hygiene with angle toothbrushprofessional oral hygiene without glycine and domiciliary oral hygiene with angle toothbrush

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • good general health (classified as ASA Physical Status ≤ 2, according to the American Society of Anesthesiology),
  • patients with implant-supported prosthetic rehabilitation completed following the Columbus Bridge Protocol at least six months prior to enrollment

You may not qualify if:

  • patients under the age of 18; heavy tobacco smokers (≥10 cigarettes per day);
  • pregnant or breastfeeding women;
  • individuals with autoimmune diseases, with or without oral tissue involvement;
  • patients presenting biological complications (such as lack of osseointegration, implant mobility, or implant loss) affecting one or more implants;
  • cases of peri-implantitis involving at least one implant; individuals with less than 40% peri-implant bone support as measured radiographically;
  • patients taking medications known to induce gingival overgrowth, as well as those undergoing corticosteroid or antibiotic therapy in the three months prior to and during the study period, or receiving antiresorptive drug therapy;
  • individuals with motor, manual, or cognitive impairments;
  • patients whose full-arch implant-supported rehabilitation had been performed at other facilities;
  • individuals with respiratory disorders; and those diagnosed with infectious diseases.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

AOU Città della Salute e della Scienza

Torino, Italy, 10126, Italy

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
FACTORIAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctor in Dental Hygiene

Study Record Dates

First Submitted

October 1, 2025

First Posted

October 8, 2025

Study Start

September 1, 2024

Primary Completion

June 1, 2025

Study Completion

June 15, 2025

Last Updated

May 5, 2026

Record last verified: 2025-09

Locations