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CompletedNCT06852599Impl_longtermUpdated Mar 6, 2025

Long-term Outcomes of Implants in Patients with Periodontitis

An observational study in Peri-Implant Health, Periodontitis and Peri-implant Mucositis, sponsored by Heidelberg University. Completed at 1 site in Germany. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-03-06.

Sponsored by Heidelberg University · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
150
Ages
18 Years and older
Sex
All
01

Study summary

The aim of the study is to examine potential influencing factors on the changes in the periodontal parameters probing pocket depth (PPD), bleeding on probing (BOP), and alveolar bone loss (ABL) on implants and control teeth (using a split-mouth design) over five (T-5), 7.5 (T-7), and ten years (T-10) of supportive periodontal care (SPC). For this purpose, 150 patients with periodontitis and implants are re-examined cross-sectionally (T0), and the changes in the main peri-implant and periodontal target parameters are compared retrospectively at the specified observation time points (T-5, T-7, T-10).

Potential influencing factors to peri-implant conditions include patient-related factors, therapy-related factors and implant-related factors. In addition, patients will be surveyed using validated questionnaires on oral health-related quality of life (OHIP-G14), and a number of common risk factors for periodontits and peri-implant conditions.

02

Conditions studied

  • Peri-Implant Health
  • Periodontitis
  • Peri-implant Mucositis
  • Peri-implantitis
03

In context

Mucositis

488 studies on the registry are indexed under Mucositis; 70 are open to participants now.

This study's enrollment of 150 is above the median of 102 across 66 observational studies indexed under Mucositis.

Browse Mucositis studies →

Lead sponsor

Heidelberg University is the lead sponsor of 279 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study cohort is recruited from patients of the Department of Conservative Dentistry at Heidelberg University Hospital who have undergone systematic periodontal therapy, have a dental implant, and meet the other inclusion criteria.

Inclusion criteria

Patient-related:

  • At least one dental implant present
  • Age ≥ 18 years at the beginning of the observation period
  • Verbal and written consent
  • Complete periodontal and dental status at one of the defined observation time points with 6 probing sites per tooth/implant and bleeding on probing (BOP) recorded during the periodontal maintenance phase

Locally:

  • a contralateral control tooth to the implant is present at the first defined observation time point
  • BOP recorded on the implant

Exclusion criteria

Exclusion Criteria:

  • No written and verbal consent
  • Younger than 18 years
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
150 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. changes in periodontal pocket depths

    Time frame: over five, 7.5, and ten years of supportive periodontal care

07

Study locations

1 site
  • Heidelberg University
    Heidelberg, Baden-Württemberg 69120, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06852599
Lead sponsor
Heidelberg University
Responsible party
Dr. Antonio Ciardo (Principal Investigator, Heidelberg University) — Principal investigator
First posted
Feb 28, 2025
Start date
Sep 1, 2023
Primary completion
May 30, 2024
Completion
May 30, 2024
Last update
Mar 6, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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