Comparison of the Efficacy of Conventional Versus Minimally Invasive Non-Surgical Periodontal Therapy in Periodontitis Patients
1 other identifier
interventional
30
1 country
1
Brief Summary
the aim of this study is to investigate the clinical outcomes of Minimally Invasive Non-Surgical Therapy(MINST) compared to Conventional non-surgical periodontal therapy (CNST)
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for early_phase_1
Started Aug 2025
Shorter than P25 for early_phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 5, 2025
CompletedFirst Submitted
Initial submission to the registry
June 16, 2026
CompletedFirst Posted
Study publicly available on registry
June 26, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 5, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 5, 2026
June 26, 2026
June 1, 2026
1 year
June 16, 2026
June 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Plaque index (PI)
1\. Plaque index (PI):The index assigns a score to each tooth based on the amount of plaque present. 0: No plaque is visible. 1. A thin film of plaque is present at the gingival margin (gumline) and can be detected with a probe. 2. Visible plaque along the gingival margin. 3. Heavy plaque accumulation in the gingival margin and interdental spaces.
basline, 1 month , 3 months
Bleeding on probing (BOP):
): "0" if no bleeding occurred within 10 second, and "1" if there was bleeding within 10 second.
baseline, 1 month , 3 months
Probing pocket Depth (PPD)
): will be measured from the gingival margin to the base of the periodontal pocket.
baseline , 1 month , 3 month
Clinical Attachment Level (CAL)
will be measured from the cement-enamel junction to the base of the periodontal pocket.
baseline ,1 month , 3 month
Study Arms (2)
conventional non-surgical periodontal therapy
EXPERIMENTALconventional mechanical debridement
Minimally Invasive Non-Surgical Therapy
EXPERIMENTALthe root surface of teeth will be thoroughly debrided by a minimally invasive approach using specific thin and delicate piezo-electric scaling tips (Woodpecker � Tip P3. Am Perfect sp. z o .• � Poland) and manual miniature periodontal curettes {� Dent Solutions. Cairo. Egypt) for reducing periodontal tissue trauma. Adjunctive use of magnification loupes will be performed.
Interventions
On the conventional non-surgical periodontal therapy side, a power-driven piezo•electric ultrasonic scaling device with scaling tips will be used the majority of the time to debride subgingival biofilm and calculus. and manual standard gracey curette instruments will be used to refine residuals from root surfaces.
Briefly. the root surface of teeth will be thoroughly debrided by a minimally invasive approach using specific thin and delicate piezo-electric scaling tips (Woodpecker � Tip P3. Am Perfect sp. z o .• � Poland) and manual miniature periodontal curettes {� Dent Solutions. Cairo. Egypt) for reducing periodontal tissue trauma. Adjunctive use of magnification loupes will be performed.
Eligibility Criteria
You may qualify if:
- Patients with stage III pericdontitis, according to the American Academy of Periodontology (AAP) and the European Federation of Periodontology (EFP) periodontal classification system .
- Medically free patients.
- Non-smokers
- Patients with good oral hygiene.
You may not qualify if:
- Pregnant or lactating females.
- Patients with systemic diseases that might affect periodontal health
- previous periodontal treatment within 6 months before baseline examination.
- prior antibiotic regimen use within 1 month before baseline examination
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Mansoura university Faculty of dentistry
Al Mansurah, Dakhlia, 00000, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- early phase 1
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD, Lecturer, Oral Medicine, Periodontology, Diagnosis, and Oral Radiology Department,
Study Record Dates
First Submitted
June 16, 2026
First Posted
June 26, 2026
Study Start
August 5, 2025
Primary Completion (Estimated)
August 5, 2026
Study Completion (Estimated)
August 5, 2026
Last Updated
June 26, 2026
Record last verified: 2026-06