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Hyaluronic Acid and Octenidine Gel as an Adjunct to Non-surgical Periodontal Treatment

Not Applicable
Not yet recruiting
Conditions
Wound Heal
Periodontal Pocket
Periodontal Attachment Loss
Periodontitis
Periodontal Inflammation
Interventions
Combination Product: Hyaluronic Acid (HA) and Octenidine gel
Procedure: Non-surgical periodontal treatment (NSPT)
Registration Number
NCT06522438
Lead Sponsor
Queen Mary University of London
Brief Summary

This parallel-group, pilot study will test the hypothesis that the adjunctive use of a thermosensitive gel containing Hyaluronic Acid (HA) and Octenidine to non-surgical periodontal treatment (NSPT) will be able to modulate the early wound healing events. This will be assessed through the expression of specific gingival crevicular fluid markers, as well as by changes in gingival blood flow (assessed by laser speckle contrast imaging), bacterial load, soft tissues contour, clinical parameters and patient-reported outcomes.

The study will involve up to 26 patients and will take place at the Centre for Oral Clinical Research (COCR), at the Institute of Dentistry, Faculty of Medicine and Dentistry, Queen Mary University of London under The Royal London Dental Hospital, Barts Health NHS Trust. Patients will be randomised to receive either NSPT alone or NSPT+ HA and Octenidine gel, and will be followed up to 3 months after treatment.

The study will consist of 7- 8 visits.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
26
Inclusion Criteria
  • Male or female aged 18 and above
  • Engaged patients presenting with a Full Mouth Plaque Score (FMPS) of ≤ 20% within the 6 weeks prior to enrolment, or exhibiting a ≥ 50% reduction in plaque score from the initial screening visit.
  • Periodontitis stage III/IV (grades A to C) with at least one site per quadrant with PPD ≥5mm, bleeding on probing and attachment loss ≥5mm
  • Willing to sign informed consent and comply with study procedures
Exclusion Criteria
  • Know hypersensitivity and/or allergy to any of the product's component (as per user leaflet)
  • Self-reported pregnancy or lactation
  • Smoking (current or in past 5 years), including e-cigarettes/vaping
  • Medical history including diabetes mellitus or other serious medical/ psychiatric conditions or transmittable diseases that according to the investigator may increase the risk associated with study participation
  • History of conditions requiring prophylactic antibiotic coverage prior to invasive dental procedures or/and systemic antibiotic therapy during the 3 months preceding the baseline evaluation
  • In chronic treatment with anti-inflammatory (including corticosteroids), anticoagulants/antiplatelets (including aspirin), immunosuppressants or other medication that can severely impact wound healing
  • History of alcohol or drug abuse
  • Subgingival professional mechanical plaque removal (excluding not-extensive subgingival debridement as judged by the examining clinician) and/or surgical periodontal treatment within the last 12 months
  • Other severe acute or chronic medical or psychiatric condition or psychological disorder, including limited mental capacity or language skills such that study information could not be understood, informed consent could not be obtained, or simple instructions could not be followed, or any additional conditions which, in the judgement of the investigator, would make the subject inappropriate for entry into this trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Test GroupNon-surgical periodontal treatment (NSPT)Non-surgical periodontal treatment (NSPT) plus Hyaluronic Acid (HA) and Octenidine gel.
Control GroupNon-surgical periodontal treatment (NSPT)Non-surgical periodontal treatment (NSPT) alone.
Test GroupHyaluronic Acid (HA) and Octenidine gelNon-surgical periodontal treatment (NSPT) plus Hyaluronic Acid (HA) and Octenidine gel.
Primary Outcome Measures
NameTimeMethod
Changes in the expression of GCF wound healing biomarkersBaseline, 1, 7, 15, 30 days and 3 months following treatment

Changes in the expression of GCF wound healing biomarkers at 1, 7, 15, 30 days and 3 months following treatment will be assessed. A subset of analytes involved in the healing process and signalling pathways such as i) inflammation/immune response (e.g., IL-1 β, IL-1 α, IL-6, IL-8, IL-4, IL-10,IL-17, TNF- α, MMP-1, MMP-8, MMP-9, TIMP-1), ii) bone formation/resorption (e.g., TGF- β, osteocalcin, osteopontin, osteoprotegerin, BMP-2), iii) oxidative stress (e.g., Myeloperoxidase), and iv) angiogenesis (e.g., VEGF, angiopoietin-1) will be selected based on the pathways identified and optimized in the genomic and proteomic work from our group. Multiplex immunoassays will be designed specifically for quantitative analyses in the GCF for the 2 groups at the different time points.

Secondary Outcome Measures
NameTimeMethod
Changes in the Blood flowBaseline and at 1, 7, 15, and 30 days following treatment.

Changes in the blood flow at 1, 7, 15, and 30 days following treatment, evaluated with Laser Speckle Contrast Imaging (LSCI)

Changes in the suppurationBaseline and at 3 months after intervention

Suppuration will be recorded as percentage of total surfaces (6 aspects per tooth), which reveal the presence of suppuration following periodontal probing. A binary score will be assigned to each surface (1 for suppuration present, 0 for suppuration absent).

Patient perception about therapy1,7 and 15 days after procedure

The extent of discomfort and/or pain experienced will be evaluated using a 100-mm visual analog scale (VAS). The anchors for each end of the scales will be designated as 0=none to 100= worst. The extent of oedema, hematoma, high fever, and interference in daily activities during the initial weeks will also be evaluated in the same way.

Changes in the bacterial loadBaseline and at 7, 15, 30 days and 3 months following treatment.

Changes in the bacterial load associated with treated sites at 7, 15, 30 days, and 3 months following intervention. Subgingival plaque samples will be analysed using next generation marker DNA sequencing to characterise the subgingival microbiota to identify and determine the levels of key periodontal bacterial pathogens and microbial community-wide changes in sites treated at the different time points.

Changes in the clinical attachment level (CAL)Baseline and at 3 months after intervention

CAL will be calculated considering the values for PPD and REC in mm

Changes in the Full mouth bleeding score (FMBS)Baseline and at 3 months after intervention

FMBS will be recorded as percentage of total surfaces (6 aspects per tooth/implant), which reveal the presence of bleeding within 10 - 30 seconds following periodontal probing. A binary score will be assigned to each surface (1 for bleeding present, 0 for bleeding absent).

Global changes in quality of life3 months after procedure

Periodontal health and quality of life following periodontal therapy will be measured through specific questionnaire at 3 months after treatment. Questionnaire will include questions to evaluate patient's perception of treatment on their periodontal health and quality of life. Patients will answer by selecting one of the following options: worsened a lot, worsened a little, stayed the same, improved a little, improved a lot, or don't know.

Changes in the gingival recession (REC)Baseline and at 3 months after intervention

REC will be measured in mm using a University of North Carolina (UNC-15) periodontal probe at six sites per tooth (i.e., mesiobuccal, buccal, distobuccal, mesiolingual, lingual, and distolingual).

Soft tissues contour changesBaseline, 1, 7, 15, 30 days, and 3 months following treatment

Soft tissues contour changes will be assessed at 1, 7, 15, 30 days, and 3 months following treatment. An intra-oral 3D scanner will be used to capture and monitor soft tissue contour changes during early phase of healing. The obtained images will be then superimposed (baseline and follow-ups) and calculation of linear and volumetric changes of the soft tissue (magnitude of the swelling, changes in shape and volume) will be performed.

Dentin hypersensitivityBaseline, 1, 7, 15, 30 days, and 3 months after procedure

A 100-mm horizontal visual analog scale (VAS) will be used to assess dentine hypersensitivity. The VAS is scored from 0= none to 100= worst dentin hypersensitivity possible and the subject will indicate the degree by marking vertically across the VAS scale.

Changes in the probing pocket depth (PPD)Baseline and at 3 months after intervention

PPD will be measured in mm using a University of North Carolina (UNC-15) periodontal probe at six sites per tooth (i.e., mesiobuccal, buccal, distobuccal, mesiolingual, lingual, and distolingual).

Changes in the Full mouth plaque score (FMPS)Baseline and at 3 months after intervention

FMPS will be recorded as a percentage of total surfaces (6 sites per tooth), which reveal the presence of plaque. A binary score will be assigned to each surface (1 for plaque present, 0 for absent).

Changes in the periodontal inflamed surface area (PISA)Baseline and at 3 months after intervention

The periodontal inflamed surface area (PISA) is expressed in mm2 and will be calculated as the sum of the PPD of BOP-positive sites for the total dentition, which can be easily calculated using routine periodontal charting.

Trial Locations

Locations (2)

Centre for Oral Clinical Research (COCR)

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London, United Kingdom

The Royal London Dental Hospital, Barts Health NHS Trust

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London, United Kingdom

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