Periodontitis Clinical Trial
Official title:
Erythritol Air-polishing Versus Curette/Ultrasonic Debridement of Mandibular Furcation Lesions in Supportive Periodontal Therapy A 12-Month Randomized Controlled Trial
NCT number | NCT04493398 |
Other study ID # | 2016/793 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 1, 2015 |
Est. completion date | December 1, 2018 |
Verified date | July 2020 |
Source | University of Bergen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Background: To effectively disrupt microbial biofilm and remove dental calculus with minimal
damage to the root surface and soft tissues with limited patient discomfort constitute a
significant tenet of periodontal therapy. The aim of the present prospective 12-month study
was to compare clinical and microbiological effects following an erythritol air-polishing vs.
conventional mechanical debridement of furcation defects in a cohort of periodontal
maintenance patients.
Methods: Twenty patients with grade II mandibular molar furcation defects volunteered to
enroll in this study. In a split-mouth design, two furcation sites in each patient were
randomly assigned to either receive subgingival debridement using erythritol air-polishing
(test) or conventional ultrasonic/curette debridement (control) at baseline, and at 3, 6, 9
and 12 months. Probing depth, clinical attachment level and bleeding on probing were recorded
at 3-month intervals. Subgingival microbiological samples obtained at baseline, 6 and 12
months were analyzed using checkerboard DNA-DNA hybridization. Discomfort from treatment was
scored at 12 months using a visual analogue scale.
Status | Completed |
Enrollment | 20 |
Est. completion date | December 1, 2018 |
Est. primary completion date | June 30, 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 80 Years |
Eligibility |
Inclusion Criteria: 1. Received supportive periodontal therapy (SPT) every 3-6 months for 2-3 years following periodontal therapy. 2. Having bilateral non-mobile, fully erupted mandibular first, second or third molars with degree II furcation defects. 3. PD=4 mm with bleeding or pus on probing. - Exclusion Criteria: 1. Mobile mandibular molars, molars with clinical or radiographic evidence of supra-/subgingival calculus or apical pathology. 2. Use of systemic antibiotics within 6 months or SPT within 3 months of study. 3. Any current medical condition affecting periodontal treatment or use of the abrasive air-polishing device. 4. Subjects with diabetes, cancer, HIV/aids, acute infections, disorders that may compromise wound healing, or pregnant women. - |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Bergen |
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* Note: There are 44 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | In 20 patients with grade II mandibular molar furcation defects, probing depth (PD) will be measured. | PD: The vertical distance from the gingival margin to the probable base of the pocket in mm. | 12 months. | |
Primary | In 20 patients with grade II mandibular molar furcation defects clinical attachment level (CAL) will be measured. | CAL: The vertical distance in mm from the cemento-enamel junction or the margin of a dental restoration to the probable base of the pocket. | 12 months. | |
Secondary | Bleeding on probing (BoP). | At site level, BoP was recorded as present upon gentle probing to the base of the vertical furcation pocket. | 12 months. | |
Secondary | Gingival crevicular fluid (GCF). | Twenty test and control sites were isolated with cottons rolls, cleaned for supragingival plaque, and air-dried. A perio paper strip was then placed 1-2 mm into the orifice of the site and left in place for 30 sec. The perio strip was inserted into the Periotron 8000® (Oraflow, Smithtown, NY, USA) calibrated to estimate the volume of GCF collected. | 12 months. | |
Secondary | Visual analogue scale (VAS). | VAS scores were used to estimate patient discomfort experienced during test and control treatment by drawing a vertical line on a 100-millimeter standardized horizontal line (0="no pain" and 100="worst pain I can imagine"). | 12 months. |
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