University of Michigan School of Dentistry
Ann Arbor, Michigan, 48109, United States
NCT Number: NCT06153212
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Ann Arbor, Michigan, 48109, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The diseased dental implant will be cleaned and the bone defect will be filled with bone graft and covered by a membrane.
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
Time frame: Baseline and 8 months after baseline surgery
Bone measurements obtained from CBCT
Time frame: 8 months after baseline surgery
To compare clinical attachment measurements using a periodontal probe from baseline to the final follow-up visit
Time frame: 8 months after baseline surgery
To compare marginal bone measurements from periapical radiographs
Time frame: 8 months after baseline surgery
To compare volumetric bone measurements of the grafted areas from CBCT
University of Michigan
Other
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
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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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