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Objectives:
The aim of this study was to evaluate in a cohort of patients with peri-implant mucositis: (a) the efficacy of professional mechanical debridement therapy assisted using Bioptron Hyperlight Therapy on the reduction of periodontal indexes (b) the reduction of total oxidative salivary stress.
Material and Methods Forty subjects with a diagnosis of peri-implant mucositis were enrolled in this study and randomly assigned to the study group (mechanical debridement therapy assisted using Bioptron Hyperlight Therapy) or control group (mechanical debridement therapy alone). The study duration was 6 months. Data on plaque index (PI), bleeding on probing (BoP), probing pocket depth (PPD) and pain relief on Visual Analogue Scale (VAS) were recorded at T0, T1 (14 days), T2 (1 month) and T3 (6 months). Group differences were assessed using Student's t-test and Pearson's Chi-squared test of homogeneity
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| peri-implant mucositis treated with standard of care-professional mechanical debridement | Active Comparator | patients with peri-implant mucositis are treated with standard of care, i.e. professional mechanical debridement |
|
| peri-implant mucositis treated with photobiomodulation in addition to standard treatment | Experimental | patients with peri-implant mucositis are treated with photobiomodulation in addition to standard treatment |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Photobiomodulation with Bioptron Hyperlight Therapy | Device | The Bioptron® Device provides polarized visible polychromatic noncoherent light with 90 W; light wavelength = 480-3400 nm; degree of polarization = 95%; specific power = 40 mW/cm2; energy density = 2.4 J/cm2. The duration of each treatment session was 10 min. Bioptron light was positioned 10 cm from the oral mucosa and a mouth opener was positioned for the entire duration of the session. Two weekly sessions during the first 4 weeks of treatment were applied. |
| Measure | Description | Time Frame |
|---|---|---|
| Periodontal chart-Probing pocket depth (PPD) | Probing pocket depth (PPD). PPD is a periodontal index. It is used to measure the depth of the tissue surrounding the dental implant; with notches measured in millimeters. The probe is placed in between the dental implant and gums and measures the depth of what is called the periodontal pocket- the space between the dental implant and the surrounding gums and bone. | Patients were assessed before study beginning (baseline) |
| Periodontal chart-Probing pocket depth (PPD) | Probing pocket depth (PPD). PPD is a periodontal index. It is used to measure the depth of the tissue surrounding the dental implant; with notches measured in millimeters. The probe is placed in between the dental implant and gums and measures the depth of what is called the periodontal pocket- the space between the dental implant and the surrounding gums and bone. | Patients were assessed at 6 weeks (T1) |
| Periodontal chart-Probing pocket depth (PPD) | Probing pocket depth (PPD). PPD is a periodontal index. It is used to measure the depth of the tissue surrounding the dental implant; with notches measured in millimeters. The probe is placed in between the dental implant and gums and measures the depth of what is called the periodontal pocket- the space between the dental implant and the surrounding gums and bone. | Patients were assessed at 12 weeks (T2) |
| Periodontal chart-Probing pocket depth (PPD) | Probing pocket depth (PPD). PPD is a periodontal index. It is used to measure the depth of the tissue surrounding the dental implant; with notches measured in millimeters. The probe is placed in between the dental implant and gums and measures the depth of what is called the periodontal pocket- the space between the dental implant and the surrounding gums and bone. | Patients were assessed at 24 weeks (T3) |
| Periodontal chart-Bleeding on probing (BOP) |
| Measure | Description | Time Frame |
|---|---|---|
| Pain relief | Pain relief assessed with the Numerical Rating Scale-11 (NRS-11) | Patients were assessed before study beginning (baseline) |
| Pain relief | Pain relief assessed with the Numerical Rating Scale-11 (NRS-11) |
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Inclusion Criteria:
Exclusion Criteria:
-
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| Name | Affiliation | Role |
|---|---|---|
| Roberto F Grassi, Prof | University of Bari Aldo Moro | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Roberto Felice Grassi | Bari | 70121 | Italy |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 35565077 | Derived | Nardi GM, Mazur M, Papa G, Petruzzi M, Grassi FR, Grassi R. Treatment of Peri-Implant Mucositis with Standard of Care and Bioptron Hyperlight Therapy: A Randomized Clinical Trial. Int J Environ Res Public Health. 2022 May 7;19(9):5682. doi: 10.3390/ijerph19095682. |
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| ID | Term |
|---|---|
| D013280 | Stomatitis |
| ID | Term |
|---|---|
| D009059 | Mouth Diseases |
| D009057 | Stomatognathic Diseases |
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| ID | Term |
|---|---|
| D028022 | Low-Level Light Therapy |
| ID | Term |
|---|---|
| D053685 | Laser Therapy |
| D013812 | Therapeutics |
| D010789 | Phototherapy |
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a randomised, double blind clinical trial
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|
Bleeding on probing (BOP). Bleeding on probing (BOP) is a parameter to measure soft tissue inflammation. It is measured with the use of a dental probe. The grading is :
|
| Patients were assessed before study beginning (baseline) |
| Periodontal chart-Bleeding on probing (BOP) | Bleeding on probing (BOP). Bleeding on probing (BOP) is a parameter to measure soft tissue inflammation. It is measured with the use of a dental probe. The grading is :
| Patients were assessed at 6 weeks (T1) |
| Periodontal chart-Bleeding on probing (BOP) | Bleeding on probing (BOP). Bleeding on probing (BOP) is a parameter to measure soft tissue inflammation. It is measured with the use of a dental probe. The grading is :
| Patients were assessed at 12 weeks (T2) |
| Periodontal chart-Bleeding on probing (BOP) | Bleeding on probing (BOP). Bleeding on probing (BOP) is a parameter to measure soft tissue inflammation. It is measured with the use of a dental probe. The grading is :
| Patients were assessed at 24 weeks (T3) |
| Periodontal chart- Plaque index (PI) | Plaque index (PI). Plaque index is used to evaluate the level and rate of plaque formation on dental implant surfaces. The grading is :
| Patients were assessed before study beginning (baseline) |
| Periodontal chart- Plaque index (PI) | Plaque index (PI). Plaque index is used to evaluate the level and rate of plaque formation on dental implant surfaces. The grading is :
| Patients were assessed at 6 weeks (T1) |
| Periodontal chart- Plaque index (PI) | Plaque index (PI). Plaque index is used to evaluate the level and rate of plaque formation on dental implant surfaces. The grading is :
| Patients were assessed at 12 weeks (T2) |
| Periodontal chart- Plaque index (PI) | Plaque index (PI). Plaque index is used to evaluate the level and rate of plaque formation on dental implant surfaces. The grading is :
| Patients were assessed at 24 weeks (T3) |
| Patients were assessed at 6 weeks (T1) |
| Pain relief | Pain relief assessed with the Numerical Rating Scale-11 (NRS-11) | Patients were assessed at 12 weeks (T2) |
| Pain relief | Pain relief assessed with the Numerical Rating Scale-11 (NRS-11) | Patients were assessed at 24 weeks (T3) |