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Effect of Different Diode Laser Power Settings as an Adjunct to Scaling and Root Planing on Clinical Periodontal Parameters and Gingival Crevicular Fluid Levels in Patients with Chronic Periodontitis

Comparative evaluation of 810 nm diode laser at various power settings as an adjunct to Scaling and Root Planing and Scaling and Root Planing alone on Gingival crevicular fluid levels of IL-1BETA and TNF-ALFHA in patients with chronic periodontitis: A split-mouth clinical study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101745
Enrollment
20
Registered
2026-01-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Laser with 1W: In every patient full mouth SRP will be performed using hand instruments (Gracey curettes) and an ultrasonic device. The laser therapy using an 810 nm diode laser with th

Sponsors

Pooja Hungund
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients who agreed to participate in the study by signing the written informed consent. 2. Patients older than 18 years with chronic periodontitis 3. Deepest probing pocket depth of 4-6 mm in at anterior or posterior teeth at each of the quadrants of the jaw. 4. Patients with no history of any periodontal treatment for at least the last 3 months. 5. Subjects who have never smoked, or who have smoked less than 100 cigarettes in their lifetime. (Glossary Of Centers for Disease Control and Prevention).

Exclusion criteria

Exclusion criteria: 1. Patients with systemic disorders that could impact the outcome and prognosis of periodontal treatment, such as diabetes mellitus. 2. Patients who had taken antibiotics or anti-inflammatory drugs within the last three months. 3. Pregnant and lactating women. 4. Patients with periodontitis stage IV (Classification of periodontitis and peri-implant diseases and condition as proposed in 2017 World Workshop).

Design outcomes

Primary

MeasureTime frame
Clinical parameters which include gingival index, bleeding on probing, probing pocket depth, clinical attachment level will be measured on the first day (Day-0) and after 3 months.Timepoint: Clinical parameters which include gingival index, bleeding on probing, probing pocket depth, clinical attachment level will be measured on the first day (Day-0) and after 3 months.

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactPooja Hungund

The Oxford Dental College

drpoojahungund@gmail.com7019971357

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026