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Clinical Trials/NCT03074565
NCT03074565
Completed
Not Applicable

Comparison of Ultrasonic Versus Hand Instrumentation Plus Ultrasonic for Effective Sanative Therapy

Brock University2 sites in 1 country42 target enrollmentMay 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Periodontitis
Sponsor
Brock University
Enrollment
42
Locations
2
Primary Endpoint
Periodontal healing evaluated based on changes in mean probing depth (mm)
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Periodontitis is a chronic oral infection that results in the breakdown of connective tissue and alveolar bone that support the teeth. Non-surgical sanative therapy using a combination treatment of hand and ultrasonic instrumentation is the primary treatment option for patients with periodontitis. However, the hand-held instrumentation requires continuous sharpening for optimal outcomes, which introduces tremendous variability as well as a large increase in time spent by the treating dental hygienists. Therefore, this study aimed to determine if ultrasonic instrumentation alone can provide similar improvements to periodontal outcomes compared to ultrasonic plus hand instrumentation.

Detailed Description

Periodontitis is a chronic oral infection that results in the breakdown of connective tissue and alveolar bone that support the teeth. Bacteria and the body's own immune system mediate the severity of periodontitis, where teeth may become loose, fall out or have to be removed. Non-surgical sanative therapy (also referred to as "deep cleaning") is the primary treatment option for patients with generalized chronic periodontitis. This includes debridement with both ultrasonic and hand instrumentation. Using this approach, surgery is avoided for 93% of patients who undergo sanative therapy at our private periodontal specialty practice (unpublished data). However, the hand-held instrumentation requires continuous sharpening for optimal performance, which introduces tremendous variability as well as a large increase in time spent by the hygienists. Ultrasonic instrumentation does not require sharpening, as a new instrument head is used for every new patient. Therefore, given the interest in "contemporary instrumentation", meaning ultrasonic therapy alone, the primary objective of this study is to determine if similar improvements in periodontal indices can be achieved using ultrasonic instrumentation alone versus ultrasonic instrumentation in conjunction with hand instrumentation. Secondary objectives included the following: i) to determine if the time required to complete sanative therapy is reduced using ultrasonic therapy alone, given the ultrasonic instruments do not require sharpening and less instrument changes by the hygienist are required during treatment. If the time is less for ultrasonic therapy alone, there is a potential cost-savings for the patient, as well as less time spent receiving therapy in the dental chair; ii) to determine if the treatment with ultrasonic therapy versus ultrasonic therapy and hand instrumentation is more comfortable for the patient; and iii) to determine if there is less sensitivity to the teeth with ultrasonic therapy alone compared to the combination of ultrasonic therapy and hand instrumentation.

Registry
clinicaltrials.gov
Start Date
May 1, 2017
End Date
February 5, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wendy E. Ward, Ph.D.

Professor

Brock University

Eligibility Criteria

Inclusion Criteria

  • Both males and females age 19 years or older who are undergoing sanative therapy for moderate to severe chronic periodontitis are eligible.
  • Chronic periodontitis has been classified as localized or generalized depending on whether \<30% or \>30% of sites are involved.
  • Severity is based on the amount of clinical attachment loss (CAL) and is designated as slight (1-2 mm CAL), moderate (3-4 mm CAL) or severe (\> 5 mm CAL).

Exclusion Criteria

  • Patients with dental implants,
  • pregnancy,
  • a recent history of antibiotic use (within 3 months prior to treatment) and
  • inability to give consent for the study.

Outcomes

Primary Outcomes

Periodontal healing evaluated based on changes in mean probing depth (mm)

Time Frame: Baseline and between 8 and 12 weeks after sanative therapy

Healing is evaluated based on changes in mean probing depth

Secondary Outcomes

  • Plaque index(Baseline and between 8 and 12 weeks after sanative therapy)
  • Bleeding on Probing(Baseline and between 8 and 12 weeks after sanative therapy)
  • Clinical Attachment Loss (Periodontal Attachment Loss)(Baseline and between 8 and 12 weeks after sanative therapy)

Study Sites (2)

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