Non-surgical Treatment of Peri-implant Pockets With H42

Recruiting Observational Study
Peri-implantitis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
25 – 65
Sex
Any
Study type
Observational
Participants needed
56 (estimated)
Sponsor
Bioteck S.p.A. · Industry
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About This Trial
This prospective, observational study evaluates the efficacy and safety of H42 non-surgical treatment for peri-implant pockets. The trial involves 56 patients, with 28 subjects receiving the H42 treatment and 28 acting as a control group to monitor soft tissue healing and bone level changes. Clinical outcomes focus on Pocket Probing Depth (PPD) and Silness and Löe Plaque Index (PI) measured at ba…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Men or women with age ≥ 25 and ≤ 65 years. * Subjects affected by peri-implant pockets with probing depth (PD) in the range between 6 to 8 mm. * Each subject can have from 1 to 5 defects. * Subjects willing to provide signed informed consent to clinical investigation participa…
Contacts

Marco Morroni, PhD

389 059 0480

m.morroni@bioteck.com

CONTACT

Anna Di Bona, PhD

32779983709

a.dibona@bioteck.com

CONTACT