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Use of Ozone Gel as an Antimicrobial in Treatment of Periodontitis

G

Ghufran Falih Hassan

Status and phase

Completed
Phase 1

Conditions

Periodontitis
Periodontal Pocket

Treatments

Drug: ozone gel

Study type

Interventional

Funder types

Other

Identifiers

NCT05905445
Ozone gel in periodontitis

Details and patient eligibility

About

Periodontitis is an inflammatory disease that destroys tooth-supporting structures through oral bacterial plaque. ozone gel's act as an antimicrobial effect as an adjunct to conventional periodontal therapy (scaling and root planning). exposure of bacteria to ozone leads to the oxidation of the phospholipids and lipoproteins that comprise the bacterial cell membrane. Ozone gel has the potential to play an anti-inflammatory role in the treatment of periodontitis by monitoring both clinical and biological parameters.

Full description

Periodontitis is an inflammatory disease that destroys tooth-supporting structures through oral bacterial plaque. Scaling and root planning are considered the gold standard treatment for periodontal disease. Antiseptics represent an aid to the gold standard nonsurgical treatment of scaling and root planning (SRP) for periodontal disease. Adjuncts to scaling and root planning have been introduced as ozone gel. This gel represents both antimicrobial and beneficial effects while expressing safe cytocompatibility toward host tissues, which is progressively developing.

The study aims to determine ozone gel's antimicrobial effect as an adjunct to conventional periodontal therapy (scaling and root planning).

Material and Methods: Twenty-one patients with periodontitis were enrolled in this study. There were 58 periodontal pockets divided into two groups by a blinded split-mouth design. The control group had 28 periodontal pockets treated with scaling and root planning only, while the test group had 30 with scaling and root planning and ozone gel. Two gel applications were applied at baseline and one month after the treatment. Plaque index, bleeding on probing, probing pocket depth, and relative attachment level were recorded. Gingival crevicular fluid samples were collected from the pockets at each site for both groups at different time intervals. The GCF sample was transferred into Eppendorf tubes containing 1.5 ml of PBS buffer, and the samples were stored in a freezer at -40˚C.

Enrollment

21 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • The patient should be systemically healthy
  • The patient has periodontitis equal to or more than two non-adjacent teeth, with probing pocket depth equal to or more than 4mm.
  • Patients capable of following orders and motivation

Exclusion criteria

  • Patients with removable dentures who undergo orthodontic therapy.
  • Patients with teeth suffer from endo-periodontal lesions.
  • Patients have three months of using anti-inflammatory medications, antibiotics, immune suppressants, or oral contraceptives.
  • Patients having systemic conditions that affect the condition.
  • Pregnant or nursing mothers.
  • Patients who are smokers

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

21 participants in 2 patient groups

ozone gel with conventional scaling and root planning
Experimental group
Description:
administered ozone gel in the probing pocket depth after scaling and root planning by a disposable plastic syringe with a blunt tip until the access ozone became out of the pocket. this procedure is made at baseline and in the first month. instructed the patient not to eat or drink for at least 30 minutes
Treatment:
Drug: ozone gel
only conventional scaling and root planning
No Intervention group
Description:
only scaling and root planning without any intervention.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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