The Effects of Diode Laser as an Adjunct to Non-surgical Periodontal Treatment on Periodontal Status in Patients With Stage III-IV Periodontitis

Mohammed Bin Rashid University of Medicine and Health Sciences

Status: Unknown

Conditions: Periodontal Diseases

Treatments: Procedure: Diode laser (device) with scaling and root planing; Procedure: Conventional scaling and root planing

Study type: Interventional

Funder types: Other

Identifiers

NCT04477551

MBRU/IRB/2020/006

Details and patient eligibility

About

Periodontal disease is serious and global chronic disease. The prevalence of periodontal diseases in United Arab Emirates is not clear but data from Dubai Health Authority showed that one in five patients has received periodontal treatment in recent years.

Several studies reported the additional benefits provided by the use of diode laser in combination with ultrasonic debridement in the treatment of gum disease. The use of diode laser may debridement of deep pocketing areas while improving healing of gum tissues.

The aim of the study is to compare the effect of removing bacterial deposit (biofilm) from deep tooth pocket using combined diode laser and conventional pocket debridement versus conventional pocket debridement alone on tooth supporting tissue parameters in patients with advanced gum disease (periodontitis).

Methodology: A total of 22 patients with advanced gum disease will be randomly allocated to two groups: a control group, which will receive conventional pocket debridement and a test group which will receive ultrasonic debridement with diode laser. Gum measurements will be recorded by a masked calibrated examiner at six points for each tooth and patients' postoperative experience and satisfaction will be assessed using special forms.

Enrollment: 22 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Aged 18 or over.
• Diagnosed with unstable generalised periodontitis, stage III-IV and grade B or C.
• Good compliance and commitment to attend follow-up review appointments.
• Willing to provide informed consent.

Exclusion criteria

• Received periodontal treatment in the last 12 months.
• Received systemic antibiotic in the last 6 months.
• Pregnancy or lactating participants

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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22 participants in 2 patient groups

Diode laser (device) with scaling and root planing

Experimental group

Description:

Diode laser (device) with conventional scaling and root planing

Treatment:

Procedure: Diode laser (device) with scaling and root planing

Conventional scaling and root planing

Active Comparator group

Description:

Conventional scaling and root planing

Treatment:

Procedure: Conventional scaling and root planing