The Efficacy of Cyanoacrylate Adhesive (PeriAcryl®90 HV) in Periodontal Wound Healing

University of British Columbia20 enrolled

Overview

Periodontal disease is a gum infection caused by plaque on teeth containing both bacteria and calculus (hard) deposits. These need to be removed on a regular basis to maintain gum health and to prevent teeth weakening. A routine cleaning procedure, scaling/root planing, is accompanied with post-operative soft tissue tenderness and teeth sensitivity making oral hygiene maintenance difficult during wound healing. The need for novel therapeutic approaches, such as cyanoacrylate adhesives, has been identified. It has been hypothesized that its application may provide comfort and assist patients with their daily oral self-care procedures following teeth cleaning.

Hypothesis: The supra-gingival marginal application of cyanoacrylate adhesive will promote periodontal wound healing and prevent the increase of sensitivity of hard (teeth) and soft (gingiva) tissues following non-surgical periodontal therapy (NSPT). This pilot study involves a small number of participants, and while it is not designed to prove causation, it will evaluate safety and efficacy. If clinical results are positive, these data may be used to determine sample and power needs for larger studies. With enhanced post-operative comfort, the patient's ability to disrupt biofilm and maintain optimal daily oral self-care can be achieved. Biofilm disruption is paramount to achieving periodontal health. Specifically, the adjunctive placement of an adhesive dressing may reduce biofilm accumulation that is associated with periodontal inflammation. This novel application could improve the patient's oral and thus overall health. The present pilot trial aims to explore the therapeutic effectiveness of a cyanoacrylate adhesive (PeriAcryl®90 HV) in reducing patient-reported outcomes related to discomfort and sensitivity post NSPT, examine their potential positive effects on periodontal wound healing as well as recording any potential side-effects that may have been experienced by the patients.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Eligibility

Sex: ALLMin age: 19 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: The potential subjects must: * Be capable of giving informed consent and 19 years of age or older * Have a minimum of 18 teeth and at least 4 measurement sites with pocket depth at least 5.0 mm with bleeding on probing in at least 2 different quadrants * Be able to understand and communicate in English, as the study cannot fund a certified interpreter * Be willing and able to return for treatment and evaluation throughout the course of this study. Exclusion Criteria: Potential subjects must not: * Have had any antibiotics in the last month * Be pregnant, nursing or plan to become pregnant over the course of the trial * Have an active smoking history (tobacco or otherwise) * Have sites with overt abscess, active caries or crown/root fractures * Have known adverse reactions or allergies to cyanoacrylates or formaldehyde * Have any other significant disease or take medication(s) that, in the opinion of the investigator, may interfere with the evaluation of safety or efficacy of cyanoacrylate and overall compliance.

Outcomes

Primary Outcomes

Prevention of increased post-operative discomfort post placement of cyanoacrylate adhesive measured by Visual Analogue Scale

Time frame: after 6-8 weeks

Change in clinical attachment levels (CAL) after NSPT with adjunctive placement of cyanoacrylate adhesive

Time frame: after 6-8 weeks

Prevention of increased hypersensitivity (hard and soft dental tissues) after NSPT post placement of cyanoacrylate adhesive measured by Visual Analogue Scale

Time frame: after 6-8 weeks

Continued relief post placement of cyanoacrylate adhesive measured by Visual Analogue Scale

Time frame: after 6-8 weeks

Secondary Outcomes

Subjects' compliance to having the cyanoacrylate adhesive post-operatively by interview and tabulation of patient-reported outcomes

Time frame: after 6-8 weeks

Number of adverse reactions to the placement of cyanoacrylate adhesive at the supra-gingival margin

Time frame: after 6-8 weeks

Change in probing pocket depth (PD)

Time frame: after 6-8 weeks

Change in bleeding on probing (BOP)

Time frame: after 6-8 weeks

Change in plaque scores

Time frame: after 6-8 weeks

Subjects' perception of having the cyanoacrylate adhesive post-operatively by interview and tabulation of patient-reported outcomes

Time frame: after 6-8 weeks

The Efficacy of Cyanoacrylate Adhesive (PeriAcryl®90 HV) in Periodontal Wound Healing

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts