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Impact of Non-surgical Periodontal Treatment of miRNome

Effects of Minimally Non-surgical Periodontal Treatment Versus Quadrantwise Subgingival Instrumentations on miRNome in Gingival Tissues

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06382935
Enrollment
60
Registered
2024-04-24
Start date
2024-04-20
Completion date
2024-10-15
Last updated
2024-04-24

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

Conditions

Periodontitis

Brief summary

A double-blind randomized-controlled clinical trial is conducted in order to evaluate the impact of non-surgical periodontal treatment by means of minimally invasive approach MINST or Q-SI (quadrantwise) approach in subjects with periodontitis on miRNome in gingival crevicular fluid

Detailed description

A double-blind randomized-controlled clinical trial is conducted in order to evaluate the impact of non-surgical periodontal treatment in subjects with periodontitis. 60 patients: 30 with periodontitis and 30 healthy controls. All the patients are assessed for clinical, periodontal, blood following of minimally invasive approach MINST or Q-SI (quadrantwise). Measurements are taken before and after initial periodontal treatment in the periodontal subjects.

Interventions

Probin Pocket Depth reduction in millimetres before and after treatment

Sponsors

University of Catania
Lead SponsorOTHER

Study design

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

Masking description

Sealed envelopes

Intervention model description

Non-surgical periodontal treatment Subgingival biofilm ultrasonic debridement with MINST or Q-SI

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Diagnosis of Periodontitis

Exclusion criteria

* Periodontal treatment * Use of antibiotics, NSAIDs, and immunosuppressants during the last 6 months * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Probing Pocket Depth6-monthsReduction in Probing Pocket Depth after treatnebt

Countries

Italy

Contacts

Primary ContactGaetano Isola
gaetano.isola@unict.it0953785652
Backup ContactRosalia Leonardi
rleonardi@unict.it0953785652

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026