Periodontal Diseases Clinical Trial
Official title:
Evaluation of Enamel Matrix Derivative as an Adjunct to Minimally Invasive Non-surgical Treatment of Intrabony Defects. A Randomized Controlled Clinical Trial.
| Verified date | June 2024 |
| Source | Aristotle University Of Thessaloniki |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Aim: The aim of this prospective, randomized, parallel arm, blind, controlled clinical trial is to compare the clinical and radiographic outcomes following regenerative treatment of intrabony periodontal defects using a Minimally Invasive Non-Surgical Technique (MINST) with or without the application of Enamel Matrix Derivative (EMD) Research Hypothesis: The hypothesis is that the adjunctive application of EMD will enhance the clinical and radiographic results of minimally invasive non- surgical treatment of intrabony defects. Radiographic bone fill will be the primary outcome of the research, whereas CAL gain and PD reduction will constitute the secondary outcomes.
| Status | Completed |
| Enrollment | 40 |
| Est. completion date | March 15, 2021 |
| Est. primary completion date | March 15, 2021 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - Be at least 18 years of age with a diagnosis of periodontitis. - Have at least one isolated interproximal intrabony defect on a single-rooted tooth or a mandibular molar not extending to the furcation area with radiographic depth ranging between 3 mm-7 mm, pocket depth and clinical attachment loss =6 mm and radiographic defect angle = 35o - Proper oral hygiene: full-mouth plaque score (FMPS) =20% ?a? full-mouth bleeding score (FMBS) =20% - Systemically healthy (absence of systemic conditions that can affect the treatment outcome of periodontal therapy) Exclusion Criteria: - Pregnant or lactating female - Current acute infection - Non- surgical periodontal treatment the last 6 months or surgical periodontal treatment the last 12 months - Teeth having an improper endodontic therapy with clinical signs of infection or subgingival restorations - Tooth mobility 2nd- 3rd degree - History of radiation therapy in the head and neck region |
| Country | Name | City | State |
|---|---|---|---|
| Greece | Aristotle University of Thessaloniki, School of Dentistry | Thessaloníki | Thessaloniki |
| Lead Sponsor | Collaborator |
|---|---|
| Aristotle University Of Thessaloniki |
Greece,
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* Note: There are 20 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Other | Recession | Recession depth calculated as the difference of clinical attachment level minus probing depth. | Change from baseline to 12 months | |
| Other | Full mouth plaque score | Percentage of tooth sites with detectable plaque | Change from baseline to 12 months | |
| Other | Full mouth bleeding score | Percentage of tooth sites with bleeding when a periodontal probe is traced along the gingival margin | Change from baseline to 12 months | |
| Other | Distance from the CEJ or the margin of a restoration to the bottom of the defect (CEJ-BD) | Measured in millimeters | Change from baseline to 12 months | |
| Other | Distance from the Cementoenamel Junction to the bone crest (CEJ-BC) | Measured in millimeters | Change from baseline to 12 months | |
| Other | Depth of the intraosseous defect | Distance from the bone crest to the bottom of the defect (BC-BD) measured in millimeters | Change from baseline to 12 months | |
| Other | Angle of the intraosseous defect | Angle will be determined by the line defined by the root surface of the involved tooth and the line defined by the bone wall of the defect | Change from baseline to 12 months | |
| Primary | Radiographic bone fill | Bone level in the intrabony defect | Change from baseline to 12 months | |
| Secondary | Clinical attachment gain | Clinical attachment level of intrabony defect measured in millimeters | Change from baseline to 12 months | |
| Secondary | Pocket depth reduction | Pocket depth of intrabony defect measured in millimeters | Change from baseline to 12 months |
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