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Controlled, randomized trial of trehalose powder in air-polishing for subgingival debridement during supportive periodontal treatment.

Controlled, randomized trial of trehalose powder in air-polishing for subgingival debridement during supportive periodontal treatment. - Crtotpiafsddspt

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00006296
Enrollment
50
Registered
2015-06-10
Start date
2015-06-15
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Chronic marginal periodontitis K05.3

Interventions

Group 1: Treatment of a periodontal pocket of at least 5 mm probing depth with an ultra sonic device for 20 sec. Microbiological out of the pocket are taken beforte and after treatment. Controles are

Sponsors

Orochemie GmbH + Co KG
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Two one-rooted teeth in the same jaw in different quadrants; probing depth at least 6mm or 5mm with BOP; no intake of antibiotics during the last 3 months; last systematic periodontitis therapy within the last 2 years

Exclusion criteria

Exclusion criteria: Probing depths under 6mm; several-rooted teeth; probing depth at least 6mm or 5mm with BOP; intake of antibiotics during the last 3 months; last systematic periodontitis therapy more than 2 years ago

Design outcomes

Primary

MeasureTime frame
attachment gain after 3 months

Secondary

MeasureTime frame
reduction of pocket probing depth, reduction of bleeding on probing (BOP), decrease of clinically healthy periodontal sites in percent (probing depth = 4mm, no bleeding) from baseline to 3 months after treatment and to 6 months after treatment.

Countries

Germany

Contacts

Public ContactJohan Peter Wölber

Klinik für Zahnerhaltungskunde und Parodontologie, Department für Zahn-, Mund- und Kieferheilkunde, Uniklinik Freiburg

johan.woelber@uniklinik-freiburg.de+49 761 48800

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 27, 2026