Clinical Effects of Photodynamic Therapy in Peri-implantitis

Not Applicable

Recruiting

• Conditions: peri implantitis.; Post-osseointegration biological failure of dental implant; M27.62

• Registration Number: IRCT20201021049104N1
• Lead Sponsor: Islamic Azad University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 November 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

18-80 years of age
Presence of at least one site with peri-implantitis (PPD= 6mm, MBL=3 mm and bleeding/suppuration on probing)
At least 1 year of function in implants
Screw type implants with rough surface

Exclusion Criteria

Use of antibacterial or non-steroidal anti-inflammatory drugs within 3 months prior to diagnosis
Implant mobility
Pregnancy or breastfeeding
History of autoimmune diseases, malignancy, cardiovascular insufficiency or acute diseases of other organs
History of peri-implantitis or periodontal treatment in last 6 months
Uncontrolled diabetes (HbA1c > 7%)
Tobacco use

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Probing pocket depth(PPD). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: plastic probe.;Clinical attachment loss(CAL). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: plastic probe.;Papillary bleeding index(PBI). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: Observation of papillary bleeding pattern.;Modified mombelli plaque index(mPI). Timepoint: at baseline, 2 weeks,1,3 and 6 month after treatment. Method of measurement: Observation.