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Treatment of Peri-implant Mucositis on Incongruous Dental Prostheses Versus Congruous

Impact of Non-surgical Treatment of Peri-implant Mucositis on Incongruous Dental Prostheses Versus Congruous on a Single Tooth Restoration

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05923554
Enrollment
56
Registered
2023-06-28
Start date
2023-05-25
Completion date
2023-10-31
Last updated
2023-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bleeding of Subgingival Space

Brief summary

The aim of the present study was to test the hypothesis that non-surgical periodontal therapy on peri-implant mucositis resolution results in a greater clinical improvement in patients with congruous versus non-congruous single dental implant restoration.

Detailed description

The aim of the present study was to test the hypothesis that non-surgical periodontal therapy on peri-implant mucositis resolution results in a greater clinical improvement in patients with congruous versus non-congruous single dental implant restoration by comparing two groups of patients with peri-implant mucositis.

Interventions

OTHERChanges in Probing Depth to non-surgical periodontal therapy

Changes in Probing Depth following non surgical periodontal treatment performed with hand and ultrasonic tips

Sponsors

University of Catania
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

After non-randomization, patients were assigned to a group with un-congruous single-tooth prostheses and a group with congruous single-tooth prostheses. Patients received a one-stage full-mouth scaling without chlorhexidine. Clinical and microbiological examination was performed at baseline, after 1, 2, and 3 months.

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* peri-implant mucositis * bleeding on probing and/or a gingival index \<1 at least at one site at baseline * absence of peri-implant bone loss during the last 2 years before baseline

Exclusion criteria

* Periodontal disease * Systemic diseases

Design outcomes

Primary

MeasureTime frameDescription
Bleeding on probing change % reduction6-monthsReduction in bleeding on probing % change following non surgical periodontal therapy

Secondary

MeasureTime frameDescription
Reduction of probing depth in mm6-monthsReduction of probing depth following non surgical periodontal therapy

Countries

Italy

Contacts

Primary ContactGaetano Isola
gaetano.isola@unict.it0953785652
Backup ContactRosalia Leonardi
rleonardi@unict.it

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026