New study tests if a collagen wrap boosts bone graft success for infected implants
NCT ID NCT05699343
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study compares two surgical treatments for peri-implantitis, a serious gum infection around dental implants. Fifty-two adults will receive either a bone graft alone or a bone graft covered with a resorbable collagen membrane. The goal is to see which method better stops infection, reduces pocket depth, and restores bone loss around the implant over five years.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Bone graft (InterOss Collagen) and collagen membrane (InterOss Collagen Guide)
- What this could lead to
- If it works, this could show that adding a collagen membrane over a bone graft improves the success rate of treating peri-implantitis, helping to save infected dental implants.
- What could go wrong
- This is a small, early-stage trial with only 52 participants, so results may not apply to everyone. The treatment is surgical and carries risks like infection, implant failure, or nerve damage.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 52 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2023
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: To be enrolled, the participant must meet the following inclusion criteria: 1. age 18 years or older 2. be patients of record at the University of Pittsburgh Periodontics Department 3. Systemically healthy patients 4. Full-mouth plaque score and full-mouth bleeding score ≤ 30% (measured at six sites per tooth) 5. Study individuals will be included if they met the following criteria: (a) one or more peri-implant sites with PPD ≥6 mm combined with BOP/suppuration, and (b) peri-implant marginal bone loss, defined as a crater like defect ≥3 mm as assessed from intra- oral radiographs, (c) Infrabony circumferential defect of more than 270° determined by CBCT, (d) crown not possible to retrieve before surgery Exclusion Criteria:study individuals will be excluded if any of the folllowing apply: 1. Unlikely to be able to comply with study procedures and unable to return to SDM for multiple appointments over the course of about a year. 2. Uncontrolled pathologic processes in the oral cavity (cancer and active periodontal disease) 3. History of allergic reactions to dental local anesthetics 4. History of head and neck chemotherapy or radiation within 5 years prior to surgery 5. Systemic or local disease or condition that could compromise post-operative healing and/or osseointegration, such as HIV infection, Paget's disease, osteoporosis, etc. 6. Reported diagnosis of diabetes mellitus 7. Patients taking corticosteroids, IV bisphosphonates, or any immunosuppressant medication that could influence post-operative healing and/or osseointegration 8. Smokes more than 10 cigarettes/day (self-reported) 9. History or current medications with known side effects of gingival growth (including any of the following: phenytoin, phenobarbital, lamotrigine, vigabatrin, ethosuximide, topiramate, primidone, nifedipine, diltazem, amlodipine, felodipine, verapamil, cyclosporine). 10. Present alcohol and/or drug abuser (self-reported) 11. Pregnant, unsure pregnancy status, or lactating females (self-reported), or planning to become pregnant within 1 year of study enrollment
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Pittsburgh School of Dental Medicine
Pittsburgh, Pennsylvania, 15213, United States
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