- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02744417
Effect of Smoking Cessation on Clinical and Microbiological Outcomes of the Non-surgical Periodontal Therapy (EsCAPE2)
Studienübersicht
Status
Bedingungen
Detaillierte Beschreibung
Smokers willing to quit, with 10 teeth or more, and with periodontitis (30% or more of their teeth with proximal attachment loss ≥ 5 mm) were enrolled in the study. All subjects received periodontal treatment and concurrent smoking cessation therapy. Smoking cessation therapy was performed by a team comprising physicians, nurses, a psychologist and dentists, and consisted of four 1-h counselling lectures, psychologist-assisted cognitive behavioral therapy, nicotine replacement therapy and medication (bupropion or varenicline). Smoking cessation motivation was reinforced by dentists at the maintenance sessions, by means of motivational interviewing techniques. Periodontal therapy consisted in full-mouth supra and subgingival scaling and root planing (with curettes and ultrasonic scaler); oral hygiene instruction and motivation and removal of intra-oral plaque retentive factors. Further, periodontal maintenance was performed every 3 months.
A single calibrated examiner, blinded to smoking status, assessed periodontal clinical outcomes (recession, pocket depth, clinical attachment level, plaque index and bleeding on probing). A structured questionnaire was applied in order to collect demographic and behavioral information. Expired carbon monoxide concentration was measured with a monoximeter, in order to validate smoking status. A pooled subgingival plaque sample was collected from the deepest periodontal pocket from each participant. The presence and quantification of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia and Treponema denticola were determined using real time - PCR (RT-PCR).
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- smokers willing to stop smoking
- >10 teeth
- periodontitis (30% or more of their teeth with proximal attachment loss ≥ 5 mm)
Exclusion Criteria:
- systemic conditions considered as risk factors for periodontal disease,
- periodontal therapy in the last 6 months
- continuous systemic use of anti-inflammatory or steroidal drugs
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Smoking cessation therapy
Non-surgical periodontal therapy and concurrent smoking cessation therapy, with Smoking cessation counseling, Nicotine replacement therapy, use of bupropion hydrochloride and varenicline
|
Multidisciplinary smoking cessation counseling, performed by a team comprising physicians, nurses, a psychologist and dentists.
It consisted of four 1-h counselling lectures delivered by physicians, psychologist-assisted cognitive behavioural therapy, and counseling provided by dentists during the active phase of the treatment and maintenance session, using motivational interviewing techniques
Full-mouth supra and subgingival scaling and root planing (with curettes and ultrasonic scaler); oral hygiene instruction and motivation and removal of intra-oral plaque retentive factors
Nicotine replacement therapy: chewing gum (Nicorette chewing gum 2-4mg) and patches (Nicorette patches 15-25mg)
Andere Namen:
bupropion hydrochloride 150mg
Andere Namen:
Varenicline 0,5mg
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in Clinical Attachment Level
Zeitfenster: baseline - 12 months
|
Change in Clinical Attachment Level (millimeters) after 12 months
|
baseline - 12 months
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Change in Gingival recession
Zeitfenster: baseline - 12 months
|
Change in Gingival recession (millimeters) after 12 months
|
baseline - 12 months
|
|
Change in Pocket depth
Zeitfenster: baseline - 12 months
|
Change in Pocket depth (millimeters) after 12 months
|
baseline - 12 months
|
|
Change in bleeding on probing
Zeitfenster: baseline - 12 months
|
Change in bleeding on probing (percentage of sites with bleeding) after 12 months
|
baseline - 12 months
|
|
Change in visible plaque
Zeitfenster: baseline - 12 months
|
Change in visible plaque (percentage of sites with visible plaque) after 12 months
|
baseline - 12 months
|
|
Prevalence and levels of Aggregatibacter actinomycetemcomitans
Zeitfenster: baseline - 12 months
|
Prevalence and levels of Aggregatibacter actinomycetemcomitans determined by means of (RT-PCR).
|
baseline - 12 months
|
|
Prevalence and levels of Porphyromonas gingivalis
Zeitfenster: baseline - 12 months
|
Prevalence and levels of Porphyromonas gingivalis, determined by means of (RT-PCR).
|
baseline - 12 months
|
|
Prevalence and levels of Tannerella forsythia
Zeitfenster: baseline - 12 months
|
Prevalence and levels of Tanerella forsythia, determined by means of RT-PCR
|
baseline - 12 months
|
|
Prevalence and levels of Treponema denticola
Zeitfenster: baseline - 12 months
|
Prevalence and levels of Treponema denticola, determined by means of RT-PCR
|
baseline - 12 months
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Claudio M Pannuti, PhD, University of Sao Paulo
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
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
- Stomatognathe Erkrankungen
- Parodontale Erkrankungen
- Mundkrankheiten
- Parodontitis
- Physiologische Wirkungen von Arzneimitteln
- Neurotransmitter-Agenten
- Molekulare Mechanismen der pharmakologischen Wirkung
- Autonome Agenten
- Agenten des peripheren Nervensystems
- Cholinerge Wirkstoffe
- Enzym-Inhibitoren
- Psychopharmaka
- Hemmer der Aufnahme von Neurotransmittern
- Membrantransportmodulatoren
- Antidepressiva
- Dopamin-Agenten
- Cytochrom-P-450-Enzym-Inhibitoren
- Ganglionäre Stimulanzien
- Nikotin-Agonisten
- Cholinerge Agonisten
- Antidepressiva, zweite Generation
- Cytochrom P-450 CYP2D6-Inhibitoren
- Hemmer der Dopaminaufnahme
- Nikotin
- Bupropion
- Vareniclin
Andere Studien-ID-Nummern
- EsCAPE2
Plan für individuelle Teilnehmerdaten (IPD)
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