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Low-level Laser Therapy as an Adjunct to Non-surgical Periodontal Treatment

U

University of Beykent

Status

Completed

Conditions

Periodontal Disease, AVDC Stage 4
Periodontal Attachment Loss
Periodontal Diseases
Periodontal Disease, AVDC Stage 3
Periodontal Inflammation

Treatments

Procedure: non-surgical periodontal treatment
Procedure: low level laser therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05233501
interventional

Details and patient eligibility

About

The present study aimed to investigate the effects of low-level laser therapy (LLLT) as an adjunct to non-surgical periodontal treatment (NSPT) on the plasminogen-activating system in Stage 3-4, Grade C periodontitis patients.

Full description

Limited data is available regarding the effects of various periodontal treatment protocols on GCF t-PA and PAI-1 levels, and the extent to which LLLT in conjunction with NSPT affects these levels in patients with Stage 3-4, Grade C periodontitis is unknown. Therefore, this study measured standard clinical outcomes and GCF t-PA and PAI-1 levels in patients with Stage 3-4 Grade, C periodontitis in order to assess the use of LLLT as an adjunct to standard NSPT.

This split-mouth study was conducted with 15 Stage 3-4, Grade C periodontitis patients and 15 healthy individuals matched for age and sex. Participants were grouped as follows: Periodontitis/NSPT (Sham); Periodontitis/NSPT+LLLT (LLLT); Periodontally Healthy (Control). LLLT was applied following NSPT and again on post-treatment Days 2 and 7. Clinical parameters were recorded at baseline (i.e. before NSPT) and on Day 30. Gingival crevicular fluid (GCF) samples were collected at baseline and during follow-up visits on Days 7, 14 and 30. GCF t-PA and PAI-1 levels were measured with ELISA.

Enrollment

15 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Stage 3-4, Grade C periodontitis (at least one site with probing depth (PD) and clinical attachment level (CAL) ≥5 mm in their incisors and/or first molars and at least 6 other teeth with similar PD and CAL measurements, with alveolar bone loss confirmed by radiography; familial aggregation;
  • presence of ≥16 teeth;
  • no periodontal treatment in the 6 months prior to data collection;
  • non-smoker

Exclusion criteria

  • systemic problems, including a medical history of cancer, rheumatoid arthritis, diabetes mellitus, or cardiovascular disease;
  • compromised immune system;
  • pregnancy, menopause, or lactation;
  • ongoing drug therapy that might affect the clinical characteristics of periodontitis;
  • use of systemic antimicrobials during the 6 weeks prior to data collection

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

15 participants in 2 patient groups

non-surgical perıodontal treatment
Sham Comparator group
Treatment:
Procedure: non-surgical periodontal treatment
non-surgical treatment+ low level laser therapy
Experimental group
Treatment:
Procedure: low level laser therapy
Procedure: non-surgical periodontal treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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