Manual Versus Sonic-powered Toothbrushing for Plaque Reduction in Patients with Peri-implant Mucositis

NCT ID: NCT06800625

Last Updated: 2025-01-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

41 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-04-15

Study Completion Date

2024-06-15

Brief Summary

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Aim: To compare the effect of manual and sonic-powered toothbrushing on biofilm control in patients with peri-implant mucositis.

Materials and methods: The study was completed with a total of 41 patients, 21 in the sonic tooth brushing group and 20 in the manual tooth brushing group. The patients' baseline, 3rd-month, 6th-month and 9th-month periodontal examination data (Modified Gingival İndex (MGI), Modified plaque index (MPI), Bleeding on the probing index (BOP), Pocket depth (PD), Gingival Recession (GR) and Gingival Biotype (GB)) were analyzed.

Detailed Description

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Conditions

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Toothbrushing Periimplant Diseases

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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1.gruop: Manuel toothbrusing

Patients with peri-implant mucositis were instructed to use manuel toothbrushing for plaque reduction.

No interventions assigned to this group

2. group: sonic-powered toothbrushing

Patients with peri-implant mucositis were instructed to use sonic-powered toothbrushing for plaque reduction.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Bleeding on probing around the implant
2. No bone loss around the implant in the radiograph
3. Having adequate keratinized gingiva around the implant
4. The presence of an implant prosthesis that was installed at least three months previously
5. No systemic disease
6. no smoke
7. No use of antibiotic medications within the previous three months

Exclusion Criteria

1. Patients with missing data and who do not allow data use
2. Smoker
3. Data from pregnant and lactating patients
4. Pocket depth around the implant is ≥ 5
5. Patients with peri-implantitis (bone loss around the implant)
6. Patients with insufficient attached gingiva around the implant
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Niğde Ömer Halisdemir University

UNKNOWN

Sponsor Role collaborator

Hacettepe University

OTHER

Sponsor Role lead

Responsible Party

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Selcen Ozcan Bulut

asist. prof

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Nigde Omer Halisdemir University, Dentistry Faculty, Periodontology Department

Niğde, Niğde Province, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2023/15

Identifier Type: -

Identifier Source: org_study_id

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