Clinical Trial

Influence of Implant Surface Decontamination on the Reconstructive Outcomes of Peri-implantitis

Active, Not Recruiting
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Summary
Two groups are aimed at being investigated in three centers (CICOM, Clinica Branemark and Clinica Joan Pi) * Test group: Group electrolytic approach (EA): Mechanical detoxification using curettes + NiTi brushes + EA (GalvoSurge) during 2 minutes * Control group: Group hydrogen peroxide (HP): Mechanical detoxification using curettes + NiTi brushes + hydrogen peroxide 5% for 2 minutes soaked in a gauze Patients´ group selection will be randomly allocated. For patients whom their personal clinical record # ends in a number from 0 to 4 will be included in the test group, while for patients whom their personal clinical record # ends from 5-9 will be included in the control group. The infra-osseous component will be regenerated using xenograft (Creos, NB) + autogenous bone in a ratio 1:1 harvested from the adjacent area. A resorbable membrane (Creos, NB) will be placed to compartmentalize the infra-osseous component following a poncho-like approach.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2022-11-11; most recent amendment 2026-06-05.
Status change: Recruiting → Active, Not Recruiting 2024-04-27
Trial Details
NCT Number NCT05615051
Lead Sponsor Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain
Conditions Peri-Implantitis
Enrollment 60 participants
Start Date 2022-01-01
Primary Completion 2024-12-10 (estimated)
Study Completion 2026-07-10 (estimated)
Updated on ClinicalTrials.gov 2026-06-08