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Clinical efficiency of adjunctive subgingival air-polishing with and without application of biologics in the non-surgical treatment of patients with periodontitis stage III/IV - a multicenter randomized clinical trial

Clinical efficiency of adjunctive subgingival air-polishing with and without application of biologics in the non-surgical treatment of patients with periodontitis stage III/IV - a multicenter randomized clinical trial - Biologics in non-surgical periodontitis therapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00037760
Enrollment
45
Registered
2025-08-26
Start date
2025-09-29
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

Periodontitis stage III and IV

Interventions

Group 1: Scaling & Rootplaning (SRP) using ultrasconic scaler and Gracey curettes Group 2: SRP + subgingival trehalose powder air-polishing (TPAP) for 20 seconds per tooth Group 3: SRP + TPAP + applic

Sponsors

Klinik für Zahnerhaltung, Parodontologie u. Präventive Zahnheilkunde, Universitätsklinikum Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • Patients with generalized Stage III or IV periodontitis • At least 18 remaining teeth • At least one single-rooted tooth in each quadrant with at least one site showing a probing depth of = 6 mm (“index tooth”) • Radiographic evidence of periodontal bone loss exceeding 33% of the root length

Exclusion criteria

Exclusion criteria: • Subgingival root surface instrumentation within the last 12 months • Use of local or systemic antibiotics within the last 4 month • Intake of medications associated with the development of gingival overgrowth • Intake of medications affecting bone metabolism (antiresorptives) • Systemic diseases known to interact with periodontal diseases or requiring prophylactic antibiotic coverage • General health risk due to an increased risk of bacteremia • Pregnancy

Design outcomes

Primary

MeasureTime frame
Change of pocket probing depth (PD), clinical attachment level (CAL) and bleeding on probing (BOP), measured 3 and 6 months after therapy compared to baseline using a pressure-calibrated periodontal probe

Secondary

MeasureTime frame
Differentiation of primary outcome parameters (PD, CAL, BOP) with regard to initial pocket probing depths (PD 4-5mm, PD = 6 mm) and number of closed pockets (pocket closure; PD = 4 mm without BOP) 3 and 6 months after therapy

Countries

Germany, Romania, Switzerland

Contacts

Public ContactJamal M. Stein

Klinik für Zahnerhaltung, Parodontologie u. Präventive Zahnheilkunde

jstein@ukaachen.de+492418088110

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026