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Enrolling by Invitation

NCT Number: NCT06153212

Regenerative Treatment of Peri-implantitis

The purpose of this study is to study the use of a new type of d-PTFE membrane called reinforced PTFE Mesh (RPM) with dental surgery. The regenerative outcomes of RPM membranes and collagen membrane for surgical reconstructive treatment of peri-implantitis (gum disease around implants) will be compared.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Michigan School of Dentistry

Ann Arbor, Michigan, 48109, United States

About this study

Peri-implantitis is an inflammatory response that leads to irreversible loss of implant supporting bone. This study will investigate the regenerative outcomes obtained with two membranes for surgical reconstructive treatment of peri-implantitis defects when the implant is submerged and primary wound closure is obtained. In one group the newly designed d-PTFE membrane with macropores, known as the RPM membrane will be utilized, which will be compared to the traditional collagen membrane used in the other group. The clinical, radiographic, and histologic outcomes for the regenerative treatment of peri-implantitis when utilizing the same bone graft in combination with either a collagen membrane or the RPM will be evaluated via a parallel-arm randomized controlled clinical trial.

32 patients with peri-implantitis will be recruited and randomized to receive peri-implantitis treatment with either a collagen membrane or an RPM membrane.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Physical status according to the American Society of Anesthesiology (ASA) I or II, which include patients who are systematically healthy or may suffer from mild to moderate, however well-controlled systemic diseases.
  • Subjects having at least one dental implant with peri-implantitis according to the definition proposed by the 2017 World Workshop on the Classification of Periodontal and Peri-Implant Diseases and Conditions (Berglundh et al., 2018):
  • Full-mouth plaque score and full-mouth bleeding score ≤ 20% (measured at four sites per tooth)
  • Correct 3-dimensional implant positioning, or buccal position ≤ 1 mm
  • Implants which have been in function for at least 6 months

Exclusion criteria

  • A clearly mal-positioned dental implant
  • Significant interproximal horizontal bone loss (more than 50% of implant fixture length)
  • A mobile dental implant
  • Presence of uncontrolled or untreated periodontal disease
  • More than 2 weeks usage of antibiotics in the past two months
  • Subjects taking medications known to modify bone metabolism or those that can interfere with the normal wound healing (such as bisphosphonates, corticosteroids, hormone replacement therapy, parathyroid hormone, denosumab, strontium ranelate, etc.), or those with uncontrolled systemic diseases or conditions that may similarly affect the patient's healing (osteoporosis, osteopenia, hyperparathyroidism, Paget's disease, uncontrolled diabetes (HBA1c > 8)).
  • Pregnant subjects or individuals attempting to get pregnant (self-reported)
  • Subjects smoking more than 10 cigarettes a day, or those with a history of drug or alcohol abuse (self-reported)
  • Subjects unable to maintain adequate oral hygiene (O'Leary plaque index more than 50%) (O'Leary et al., 1972)
  • Any other contraindications for undergoing periodontal surgery

Treatment and study plan

Membrane placement with bone grafting

Procedure

The diseased dental implant will be cleaned and the bone defect will be filled with bone graft and covered by a membrane.

Primary outcomes

  1. Probing depth measurements in millimeters

    Time frame: About 5 weeks before baseline surgery and at 8.5 months after baseline surgery.

    To compare probing depth measurements using a periodontal probe after peri-implantitis treatment

  2. Bone measurements in millimeters

    Time frame: Baseline and 8 months after baseline surgery

    Bone measurements obtained from CBCT

Secondary outcomes

  1. Clinical attachment levels in millimeters

    Time frame: 8 months after baseline surgery

    To compare clinical attachment measurements using a periodontal probe from baseline to the final follow-up visit

  2. Marginal bone levels in millimeters at the implant site

    Time frame: 8 months after baseline surgery

    To compare marginal bone measurements from periapical radiographs

  3. Volumetric changes of grafted area in cubic millimeters

    Time frame: 8 months after baseline surgery

    To compare volumetric bone measurements of the grafted areas from CBCT

Sponsors and collaborators

Lead sponsor

University of Michigan

Other

Collaborators

  • Osteogenics Biomedical

Registry information

Official study title

Regenerative Treatment of Peri-implantitis: A Comparison of the Reinforced PTFE Mesh (RPM) and the Collagen Membrane in the Submerged Approach: a Randomized Controlled Clinical Trial

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Dec 1, 2023
Registry last updated
Jul 2, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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