- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02168621
Intervention Study of Two Protocols for Non-surgical Treatment of Chronic Periodontitis
Approaches to Pocket/Root Debridement for Periodontal Infection Control - a Study on Effectiveness.
Treatment directed towards the control of periodontal infections is to about 90% non-surgical procedures. There is evidence from a large number of randomized controlled studies that the efficacy in terms of clinical outcomes of a full-mouth ultrasonic debridement approach (FMUD) is comparable to that of traditional section-wise scaling and root planing (SRP). A hypothesis for the current effectiveness study is that comparable clinical effects will be obtained with the FMUD approach as with conventional section-wise SRP, but with significantly more favourable patient-centred and health-economic outcomes.
This randomized study involves about 100 professionals (dental hygienists) and more than 850 patients at 40 dental clinics in the Vastra Gotaland Region, Sweden. The project not only evaluate treatment effects in terms of pertinent clinical outcomes, it also has a strong focus on patient-centered measures - patient-reported experience measures (PREM) and patient-reported outcome measures (PROM) - as well as health-economics.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
All patients with chronic periodontitis (age 30 years and older) attending the selected Public Dental clinics in VG are eligible. The patients should have at least 8 teeth with pathological pockets (probing pocket depth ≥5 mm and bleeding on probing). Only patients providing signed informed consent are included.
Reported data in the study by Wennström et al. (J Clin Periodontol 2005) were used for power calculation. Thus, a total sample of 834 patients will provide a power of 95% at a significance level of p<0.05 to detect a difference of 5% in proportion of sites with "pocket closure" i.e. PPD ≤4 mm and BoP negative (primary efficacy variable) between treatment groups. For a power of 80% a total sample of 506 patients is required.
Studientyp
Einschreibung (Voraussichtlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
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Gothenburg, Schweden, SE 405 30
- Dept of periodontology, Institute of odontology, The Sahlgrenska academy at University of Gothenburg
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- chronic periodontitis
- at least 6 teeth with approximal probing pocket depth ≥5 mm and bleeding on probing
Exclusion Criteria:
- subgingival instrumentation within 6 months prior to screening examination
- compromised medical conditions requiring prophylactic antibiotic coverage
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Aktiver Komparator: Full-mouth ultrasonic debridement
Motivation and instruction in proper oral hygiene.
Before initiation of the subgingival debridement the patient must show sufficient self-performed infection control (full-mouth plaque score <30%).
One session of full-mouth ultrasonic pocket/root debridement using a piezoceramic ultrasonic instrument.
A follow-up visit after 2-4 weeks is scheduled for oral hygiene control and re-motivation/re-instruction if indicated.
At 3 and 6 months re-evaluation is performed and re-instrumentation of all sites showing a remaining probing pocket depth of ≥5 mm carried out.
Final evaluation at 18 months.
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Motivation and instruction in proper oral hygiene.
Before initiation of the subgingival debridement the patient must show sufficient self-performed infection control (full-mouth plaque score <30%).
One session of full-mouth ultrasonic pocket/root debridement using a piezoceramic ultrasonic instrument.
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Aktiver Komparator: Section-wise scaling and root planing
Conventional treatment approach comprising motivation, oral hygiene instructions and section-wise scaling and root planing at required number of consecutive appointments with 1-2 week interval.
Follow-up 2-4 weeks after the last session of SRP for oral hygiene control and re-instruction if indicated.
At 3 and 6 months re-evaluation is performed and re-instrumentation of all sites showing a remaining pocket depth of ≥5 mm carried out.
Final evaluation at 18 months.
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Conventional treatment approach comprising motivation, oral hygiene instructions and section-wise scaling and root planing at required number of consecutive appointments with 1-2 week interval.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
"Periodontal pocket closure"
Zeitfenster: Up to 18 months
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Frequency of sites with probing pocket depth (PPD) ≤4 mm and no bleeding
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Up to 18 months
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Probing pocket depth
Zeitfenster: Up to 18 months
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Reduction in mean Probing pocket depth
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Up to 18 months
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Bleeding on pocket probing (BoP)
Zeitfenster: Up to 18 months
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Reduction in frequency of bleeding on pocket probing (BoP)
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Up to 18 months
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Patient-reported outcome measures (PROM)
Zeitfenster: Up to 18 months
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Questionnaire
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Up to 18 months
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Patient-reported experience measures (PREM)
Zeitfenster: Up to 18 months
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Questionnaire
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Up to 18 months
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Investment for treatment
Zeitfenster: Up to 18 months
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Individual investment for treatment - Direct and subsidiary costs
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Up to 18 months
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Plaque score
Zeitfenster: Up to 18 months
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Percentage of tooth surfaces with bacterial deposits
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Up to 18 months
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Treatment time
Zeitfenster: Up to 18 months
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Treatment time in minutes for mechanical instrumentation and oral hygiene instructions respectively
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Up to 18 months
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Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Jan L Wennstrom, Dept of periodontology, Sahlgrenska academy, University of Gothenburg, Sweden
- Studienleiter: Maria Welander, Dept of periodontology, Sahlgrenska academy, University of Gothenburg, Sweden
- Studienleiter: Kajsa H Abrahamsson, Dept of periodontology, Sahlgrenska academy, University of Gothenburg, Sweden
Publikationen und hilfreiche Links
Allgemeine Veröffentlichungen
- Tomasi C, Liss A, Welander M, Alian AY, Abrahamsson KH, Wennstrom JL. A randomized multi-centre study on the effectiveness of non-surgical periodontal therapy in general practice. J Clin Periodontol. 2022 Nov;49(11):1092-1105. doi: 10.1111/jcpe.13703. Epub 2022 Jul 27.
- Liss A, Wennstrom JL, Welander M, Tomasi C, Petzold M, Abrahamsson KH. Patient-reported experiences and outcomes following two different approaches for non-surgical periodontal treatment: a randomized field study. BMC Oral Health. 2021 Dec 15;21(1):645. doi: 10.1186/s12903-021-02001-4.
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Voraussichtlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- VGR 2013-2
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