Monitoring of peri-implant health in patients who have undergone rehabilitation with Arcsys implants

Longitudinal assessment of peri-implant health in patients rehabilitated with implants: a prospective observational cohort study

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

REBEC

Registry ID

RBR-4w2h9rc

Enrollment

116

Registered

2026-07-16

Start date

2026-06-29

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Mucositis

Interventions

This is a prospective observational study to be conducted at the Center for Dental Research and Implants at the Federal University of Santa Catarina. In this study, patients receiving care at the cent

Eligibility

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients over the age of 18; who have had an implant in place for at least 1 year; who have at least one prosthetically restored dental implant, with a temporary or permanent prosthesis; and who are able to comply with the visit schedule established in the peri-implant maintenance program

Exclusion criteria

Exclusion criteria: Patients with dental implants without prosthetic restoration; or those with implants restored with non-functional dental prostheses

Design outcomes

Primary

Measure	Time frame
The study aims to determine the incidence of peri-implant mucositis over the 5-year follow-up period, with peri-implant mucositis defined as the presence of bleeding on probing, with or without pus, in at least one implant, in the absence of progressive radiographic bone loss compared to the baseline assessment	—

Secondary

Measure	Time frame
The study aims to determine the incidence of peri-implantitis, defined by the presence of bleeding on probing and/or pus, an increase in probing depth compared to the baseline assessment, and radiographic evidence of progressive bone loss;We expect to determine the survival rates of implants and implant-supported restorations using the Kaplan-Meier method, defining an event as the removal of the implant or prosthesis for any reason. The success of the restorations will be defined as the functional maintenance of the restoration in the absence of clinically relevant biological or mechanical complications throughout the follow-up period;The study aims to determine the association between peri-implant outcomes and potential risk and protective factors, including systemic conditions, medication use, smoking, parafunctional habits, implant characteristics, type of prosthetic restoration, width and thickness of the peri-implant mucosa, radiographic parameters, implant-to-crown ratio, and patient-centered variables	—

Measure

Time frame

The study aims to determine the incidence of peri-implantitis, defined by the presence of bleeding on probing and/or pus, an increase in probing depth compared to the baseline assessment, and radiographic evidence of progressive bone loss;We expect to determine the survival rates of implants and implant-supported restorations using the Kaplan-Meier method, defining an event as the removal of the implant or prosthesis for any reason. The success of the restorations will be defined as the functional maintenance of the restoration in the absence of clinically relevant biological or mechanical complications throughout the follow-up period;The study aims to determine the association between peri-implant outcomes and potential risk and protective factors, including systemic conditions, medication use, smoking, parafunctional habits, implant characteristics, type of prosthetic restoration, width and thickness of the peri-implant mucosa, radiographic parameters, implant-to-crown ratio, and patient-centered variables

—

Countries

Contacts

Public ContactGabriel Magrin

Universidade Federal de Santa Catarina

glmagrin@gmail.com+55 (48) 3721 9077

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Aug 10, 2026