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Enrolling by invitationNCT07809334Bony defectsUpdated Sep 9, 2026

Implant Survival After Surgical Treatment of Peri-implantitis of Infra-bony Defects

An observational study in Peri-implantitis, sponsored by University of Turin, Italy. Enrolling by invitation at 1 site in Italy. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-09.

Sponsored by University of Turin, Italy · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
75
Ages
18 Years and older
Sex
All
01

Study summary

To report the 10 years outcomes of a reconstructive surgical protocol for peri-implantitis defects with different morphologies, by means of deproteinized bovine bone mineral with 10% collagen (DBBMC).

Read the detailed description

The original population of this case series consisted of 75 patients with one crater-like defect and probing depth (PD) ≥6 mm. After flap elevation, defects were assigned to one characteristic class and treated by means of DBBMC. Following healing, patients were enrolled in an individualized supportive periodontal/ peri-implant (SPT) program.

02

Conditions studied

  • Peri-implantitis

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Keywords

  • Peri-implantitis
  • Surgical treatment
03

Who can participate

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

Study population

Subjects rehabilitated with oral dental implants who presented a single peri-implantitis crater-like lesion with a PD of ≥6 mm

Inclusion criteria

  • Patients rehabilitated with oral dental implants affected by peri-implantitis
  • A single peri-implantitis crater-like lesion with a Probing depth ofof ≥6 mm
  • No implant mobility,
  • Smokers

Exclusion criteria

Exclusion Criteria:

  • Probing depth \<6 mm;
  • Class II defects (characterized by consistent horizontal bone loss);
  • Multiple defects;
  • Implant mobility;
  • Subjects not interested in participating in the study;
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
75 participants (estimated)
Target follow-up
10 Years
Patient registry
Yes

Groups and cohorts

  • Patients rehabilitated with a dental implants affected by a crater-like defect

    Subjects, who presented a single peri-implantitis crater-like lesion with a PD of ≥6 mm and no implant mobility. Exclusion criteria were as follows: 1. PD \<6 mm; 2. Class II defects (characterized by consistent horizontal bone loss); 3. Multiple defects; 4. Implant mobility; 5. No interest in participating in the study; 6. Implants placed by other clinicians.

    Procedure: Reconstructive therapy

Interventions

  • ProcedureReconstructive therapy

    Intervention: Following the elevation of a muco-periosteal flap, all granulation tissue was completely removed from the defect area, by means of titanium curettes and a titanium brush under irrigation. Consequently, implant surfaces were covered with EDTA 24% for 2 min and chlorhexidine 1% gel for 2 min. Thereafter, the infrabony defects were filled with a deproteinized bovine bone mineral with 10% collagen. All patients were asked to follow an individualized supportive care program.

05

What researchers measure

Primary outcomes

  1. Implant survival rate

    Clinical Examination: Number of implants treated for peri-implantitis present in the oral cavity at the latest follow-up over the overall number of implants treated, expressed in %

    Time frame: From enrollment to the end of treatment at the 10-year follow-up visit

  2. Implant survival rate

    Percentage of implants still in place after surgical intervention

    Time frame: 10-year

06

Study locations

1 site
  • S.C. Chirurgia Maxillo-facciale U
    Torino, Italy
07

References and documents

Publications

  • Roccuzzo M, Mirra D, Pittoni D, Ramieri G, Roccuzzo A. Reconstructive treatment of peri-implantitis infrabony defects of various configurations: 5-year survival and success. Clin Oral Implants Res. 2021 Oct;32(10):1209-1217. doi: 10.1111/clr.13818. Epub 2021 Aug 16. PubMed 34352140 ↗

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT07809334
Lead sponsor
University of Turin, Italy
Responsible party
Sponsor
First posted
Sep 9, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Jun 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Sep 9, 2026

Oversight

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

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