Periodontal Treatment With Diode Laser in the Patients With Diabetes Melitus

Çanakkale Onsekiz Mart University

Status: Completed

Conditions: Diabetes Mellitus; Periodontal Disease

Treatments: Device: Control group; Device: Laser group

Study type: Interventional

Funder types: Other

Identifiers

NCT03444363

2013/104

Details and patient eligibility

About

This study aimed to investigate the effects of diode laser (DL) in addition to non-surgical periodontal treatment on periodontal parameters, systemic inflammatory response, and serum hemoglobin A1c (HbA1c) level in patients with uncontrolled type 2 diabetes mellitus (T2DM) and chronic periodontitis.

Full description

This study was designed as a randomized, controlled, full-mouth, 6-month clinical trial. 37 patients (20 women and 17 men) with uncontrolled T2DM and chronic periodontitis who were selected from among those admitting to Dentistry Faculty of Inonu University and Turgut Ozal Medical Center completed this study. The patients were divided into two groups. The individuals in the control group underwent placebo laser treatment in addition to scaling and root planing (SRP). The individuals in the study group underwent DL (1 W power) in addition to SRP. Clinical index measurements were performed before treatment (T0), 3 months after treatment (T1), and 6 months after treatment (T2). Plaque index (PI), gingival index (GI), bleeding on probing (BOP), clinical attachment level (CAL), and probing depth (PD) were measured to determine periodontal status. HbA1c and C-reactive protein (CRP) levels were also analyzed using blood samples.

Enrollment: 40 patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Having a diagnosis of type-2 DM according to the ADA criteria for at least two years before the study, HbA1c⩾7%,28
• Having no change in antidiabetic drugs in the last 3 months,
• Having no major diabetes complications (because chronic complications of diabetes complicate metabolic control),
• Presence of generalized CP,29
• Presence of an area with a pocket depth of 4-7 mm in at least four teeth in the upper jaw,
• Presence of at least 20 teeth in the mouth,
• Having no any systemic illness except for DM,
• Having no smoke,
• Receiving no periodontal treatment in the last 12 months,
• Receiving no antibiotics or anti-inflammatory drugs for a long period in the last 6 months,
• Not being pregnant or not to breastfeed,
• Having no third molars.

Exclusion criteria

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

40 participants in 2 patient groups

Study group

Experimental group

Description:

SRP plus diode laser (810 nm wavelength, 1 W power)

Treatment:

Device: Laser group

Control group

Active Comparator group

Description:

SRP plus placebo

Treatment:

Device: Control group