🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07644975
Starting soon Not applicable

Electrolytic Surface Decontamination in the Surgical Treatment of Peri-implantitis: A Randomized Clinical Trial

NCT07644975 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-01
Last updated
2026-06-12

Condition(s) studied

Peri-implantitis

Investigational drug(s) / intervention(s)

Electrolytic Surface DecontaminationConventional Surgical Treatment

Electrolytic Surface Decontamination: Electrolytic implant surface decontamination performed using the GalvoSurge system as an adjunct to conventional surgical treatment. The procedure is intended to remove biofilm and contaminants from the implant surface through an electrolytic cleaning process.

Conventional Surgical Treatment: Conventional surgical treatment of peri-implantitis consisting of flap elevation, mechanical implant surface decontamination using a titanium brush, and hydrogen peroxide application according to the study protocol.

Study summary

The goal of this clinical trial is to learn whether adjunctive electrolytic surface decontamination can improve the outcomes of surgical treatment of peri-implantitis. The main questions it aims to answer are:

* Does electrolytic surface decontamination reduce probing pocket depth more effectively than conventional surgical treatment alone?
* Does electrolytic surface decontamination improve bleeding on probing, suppuration, and radiographic bone levels?

Researchers will compare conventional surgical treatment plus electrolytic surface decontamination with conventional surgical treatment alone.

Participants will:

* Receive surgical treatment for peri-implantitis
* Be randomly assigned to one of the two treatment groups
* Attend follow-up visits for clinical and radiographic examinations
* Undergo assessment of probing pocket depth, bleeding on probing, suppuration, and bone level changes during follow-up

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Adults aged 18 years or older Diagnosis of peri-implantitis requiring surgical treatment Presence of at least one dental implant diagnosed with peri-implantitis Ability and willingness to attend follow-up visits Provision of written informed consent Exclusion Criteria: Pregnancy or lactation Uncontrolled systemic diseases that may affect healing Immunosuppressive therapy History of head and neck radiotherapy Current use of medications known to affect bone metabolism Inability to comply with the study protocol or follow-up schedule Previous surgical treatment of peri-implantitis at the study implant site

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Istanbul University Faculty of Dentistry Istanbul Turkey (Türkiye)
Istanbul University Faculty of Dentistry Istanbul Turkey (Türkiye)

More Istanbul University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07644975 on ClinicalTrials.gov ↗ ← All trials in Turkey