Home-Applied Dual-Light Photodynamic Therapy in the Treatment of Stable Chronic Periodontitis (HOPE-CP)-Three-Month Interim Results
A single-site, randomized clinical trial was designed to determine the efficacy of regular home use of Lumoral<sup>®</sup> dual-light antibacterial aPDT in periodontitis patients. For the study, 200 patients were randomized to receive non-surgical periodontal treatment (NSPT), including...
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Format: | Book |
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MDPI AG,
2022-11-01T00:00:00Z.
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Summary: | A single-site, randomized clinical trial was designed to determine the efficacy of regular home use of Lumoral<sup>®</sup> dual-light antibacterial aPDT in periodontitis patients. For the study, 200 patients were randomized to receive non-surgical periodontal treatment (NSPT), including standardized hygiene instructions and electric toothbrush, scaling and root planing, or NSPT with adjunctive Lumoral<sup>®</sup> treatment. A complete clinical intraoral examination was conducted in the beginning, at three months, and at six months. This report presents the three-month results of the first 59 consecutive randomized subjects. At three months, bleeding on probing (BOP) was lower in the NSPT + Lumoral<sup>®</sup>-group than in the NSPT group (<i>p</i> = 0.045), and more patients in the NSPT + Lumoral<sup>®</sup>-group had their BOP below 10% (54% vs. 22%, respectively, <i>p</i> = 0.008). In addition, patients in the NSPT + Lumoral<sup>®</sup>-group improved their oral hygiene by visible-plaque-index (<i>p</i> = 0.0003), while the NSPT group showed no statistical improvement compared to the baseline. Both groups significantly reduced the number of deep periodontal pockets, but more patients with a reduction in their deep pocket number were found in the NSPT + Lumoral<sup>®</sup> group (92% vs. 63%, <i>p</i> = 0.02). Patients whose number of deep pockets was reduced by 50% or more were also more frequent in the NSPT + Lumoral<sup>®</sup>-group (71% vs. 33%, <i>p</i> = 0.01). Patients with initially less than ten deep pockets had fewer deep pockets at the three-month follow-up in the Lumoral<sup>®</sup> group (<i>p</i> = 0.01). In conclusion, adjunctive use of Lumoral<sup>®</sup> in NSPT results in improved treatment outcomes at three months post-therapy. |
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Item Description: | 10.3390/dj10110206 2304-6767 |