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Minimally Invasive Non Surgical Therapy Versus Conventional Scaling and Root Planing for Treatment of Periodontitis

Split Mouth Comparison of Minimally Invasive Non Surgical Therapy Versus Conventional Scaling and Root Planing for Treatment of Periodontitis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04036513
Acronym
MINST
Enrollment
20
Registered
2019-07-29
Start date
2019-04-02
Completion date
2021-04-02
Last updated
2021-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Periodontal Diseases

Keywords

Periodontitis, MINST, Scaling and root planing, Split mouth, 3D analysis

Brief summary

Minimally invasive non-surgical therapy (MINST) is a new approach towards regeneration of deep periodontal defects. Important part of MINST procedure, besides usage of magnification loupes and piezo-electric devices seems to be the usage of special mini-curettes, originally mini-five and after mini-five of Hu-Friedy. So far only descriptive data about the clinical effects of such procedure are available and comparative studies that would include other treatment alternatives are lacking. Therefore, the aim of our study is, on split-mouth model, to compare the number of diseased sites (defined by probing depth ˃ 4 mm and bleeding on probing) after conventional non-surgical therapy and MINST with the usage of special mini-curettes. In addition, new 3D parameters obtained from 3D optical scanning will be developed for evaluation of volume changes of soft tissues.

Interventions

PROCEDUREMINST

For reducing the need of surgical treatment in patients with chronic periodontal disease, we will use specifically designed Hu-Friedy curettes mini five, micro mini five and after five together with piezoelectric device with thin and delicate tips that produce less periodontal trauma than usual Gracey curettes.

PROCEDUREConventional SRP

Scaling and root planing with conventional instruments.

Sponsors

University of Ljubljana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Evaluator different to care provider

Intervention model description

Split mouth - experimental and control side in the same individual Side selection will be randomized

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* periodontitis Stage III, grade B/C * at least 20 teeth * at least 9 teeth (excluding molars) in the upper jaw * without FPD, implants * without occlusal trauma signs * no pathology of endodontic origin * without chronic systemic diseases * no periodontal treatment in the last 6 months

Exclusion criteria

* poor oral hygiene (PI \> 20% at evaluation) * antibiotic treatment in the last 6 months or during the observation period * pregnant women, lactation, serious chronic systemic diseases, medication with known influence on periodontium or wound healing

Design outcomes

Primary

MeasureTime frameDescription
Number of diseased sites3 months, 6 months, 12 monthsDifference in No of Sites with PPD (probing pocket depth) \> 4 mm and BOP (bleeding upon probing)

Secondary

MeasureTime frameDescription
PPD3 months, 6 months, 12 monthsAverage probing pocket depth
CAL3 months, 6 months, 12 monthsClinical attachment loss
REC3 months, 6 months, 12 monthsGingival recession
VOL1 week, 1 month, 3 months, 6 months, 12 monthsVolumetric 3D differences evaluated by optical scanning

Countries

Slovenia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026