Use of Various Laser Systems in Peri-implatit

Peri-Implantitis Clinical Trial

Official title:

Effect of Various Laser Systems in Smokers and Nonsmokers With Peri-implantitis: A Randomized, Prospective, Single-Blind Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04826783
• Other study ID #: Interventional
• Status: Recruiting
• Phase: N/A
• Start date: April 25, 2021
• Est. completion date: April 25, 2022

Study information

• Verified date: March 2021
• Source: Kirikkale University
• Contact: kubilay baris
• Phone: 05539736477
• Email: dt.bkubilay[@]gmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Objectives: In recent years, a new field of work has been created with the use of laser beam to provide titanium surface decontamination. The aim of this study was to evaluate the effect of various laser systems in smokers and non-smokers with peri-implantitis. Materials and Methods: According to the study protocol, patients, who were diagnosed with peri-implantitis based on the clinical and radiographic evaluations, were divided into six groups: Group 1: smokers undergoing diode laser application; Group 2: smokers undergoing Erbium, chromium: yttrium, scandium, gallium, garnet (Er, Cr:YSGG) laser application; Group 3: smokers undergoing Erbium:yttrium-aluminum-garnet (Er:YAG) laser application; Group 4: non-smokers undergoing diode laser application; Group 5: non-smokers undergoing Er, Cr:YSGG laser application; and Group 6: non-smokers undergoing Er:YAG laser application. Peri-implant sulcus depth (SD), clinical attachment level (CAL), suppuration, modified plaque index (mPI), gingival index (GI), and modified sulcus bleeding index (mSBI) were recorded and peri-implant sulcus fluid (PISF) was collected to evaluate osteocalcin.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 50
• Est. completion date: April 25, 2022
• Est. primary completion date: October 25, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 60 Years

Eligibility

Inclusion Criteria:

1. Presence of pocket in probing depth of =4 mm in at least one implant

2. No mobility in implant

3. Implants with bridge foot and opposite occlusion

4. Having no systemic disease that may affect the outcome of treatment

5. No systemic use of antibiotics for the last six months

6. Not receiving peri-implantitis treatment for the last three months

7. Individuals at the 30-60 years of age.

Exclusion Criteria:

1. Individuals who did not agree to participate in the study

2. Individuals receiving radiation therapy

3. Individuals using alcohol

4. Presence of pregnancy and lactation period

5. Individuals with parafunctional habits such as clenching or bruxism.

Related Conditions & MeSH terms

• Peri-Implantitis

Intervention

Device:
• Lasers
The laser tip was applied as vertical and horizontal scan along the subgingival implant . The procedure was carried out on day zero, seven and 14.

Locations

Country	Name	City	State
Turkey	Kirikkale University faculty of Dentistry	Yahsihan	Kirikkale

Sponsors (1)

Lead Sponsor	Collaborator
Kirikkale University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sulcus depth		basaline - six month