Impact of Minimally Invasive Non-surgical Periodontal Treatment on Infrabony Defects
NCT ID: NCT06992219
Last Updated: 2025-05-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
52 participants
INTERVENTIONAL
2022-10-01
2024-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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MINST non surgical periodontal treatment
MINST non surgical periodontal treatment Periodontitis patients treated by means of MINST for infrabony defects. Patients were treated with non-surgical MINST periodontal treatment in a single session.
Non surgical periodontal treatment evaluated through probing pocket depth reduction
Patients were treated with Minimally invasive non surgical treatment (MINST) or quadrant-subgingival instrumentation (Q-SI). The efficacy of treatment in both groups was evaluated through Probin Pocket Depth reduction in millimetres measurement before and after treatment.
Q-SI non surgical periodontal treatment
Periodontitis patients treated by means of Q-SI. Patients were treated with non-surgical quadrantwise periodontal treatment in 4 sessions, 1 session per week.
Non surgical periodontal treatment evaluated through probing pocket depth reduction
Patients were treated with Minimally invasive non surgical treatment (MINST) or quadrant-subgingival instrumentation (Q-SI). The efficacy of treatment in both groups was evaluated through Probin Pocket Depth reduction in millimetres measurement before and after treatment.
Interventions
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Non surgical periodontal treatment evaluated through probing pocket depth reduction
Patients were treated with Minimally invasive non surgical treatment (MINST) or quadrant-subgingival instrumentation (Q-SI). The efficacy of treatment in both groups was evaluated through Probin Pocket Depth reduction in millimetres measurement before and after treatment.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Use of antibiotics, NSAIDs, and immunosuppressants during the last 6 months
* Pregnancy
18 Years
75 Years
ALL
No
Sponsors
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University of Catania
OTHER
Responsible Party
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Gaetano Isola
Associate Professor
Principal Investigators
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Gaetano Isola, DDS
Role: PRINCIPAL_INVESTIGATOR
Università degli Studi di Catania
Locations
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AOU Policlinico G. Rodolico
Catania, , Italy
Countries
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Other Identifiers
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2024-3308
Identifier Type: -
Identifier Source: org_study_id
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