MedTrace Logo

Evaluation of Fractalkine and Its Receptor in Peri-implantitis

NCT06685523 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2024-11-12

No results posted yet for this study

Summary

In this study, mechanical debridement group, Er:YAG laser group and diode laser group will be compared in terms of reducing peri-implant sulcus depth in the treatment of peri-implantitis.

Conditions

  • Peri-implantitis

Interventions

PROCEDURE

Subgingival debridement

To be applied 1 times (0. days)

PROCEDURE

Er:YAG laser decontamination

To be applied 3 times

PROCEDURE

Diyot laser decontamination

To be applied 3 times

Sponsors & Collaborators

  • Kubilay BARIŞ

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-11-08
Primary Completion
2025-05-08
Completion
2025-05-15

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06685523 on ClinicalTrials.gov