Effect of Toothpaste on the Reduction of Plaque and Inflammation
Clinical Evaluation of the Effect of an Experimental Toothpaste on the Reduction of Dental Plaque and Gingival Inflammation
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Szczegółowy opis
Before study start, investigators and study nurses will be trained on how to apply SOPs, parameters, and adverse event management. On-site monitoring will be done by the sponsor after recruitment, after visit 2 and after the final visit.
All source data will be entered in paper CRFs. For the statistical analysis these data will be entered into the data bank via double data entry. Programmed range checks, validity checks, consistency checks, and manual/visual data checks for medicinal plausibility will be done before the blind data review meeting. During blind data review meeting minor protocol violations will be recorded and assessed. No imputation of missing data will be done for ITT or PP analyses.
The sample size estimation was carried out by means of one-sided unpaired t-test with a one-sided significance level of α=0.05. For testing superiority of the test product over negative control, the investigators test the hypothesis, H0: μTest product - μNegative control ≤ 0 H1: μTest product - μNegative control > 0 by using a one-sided t-test with α=0.05. A relevant difference of Δ=0.14 and a standard deviation of σ=0.4 was assumed based on previous studies. When estimating a drop-out rate of about 20 % a total of 120 = 102 + 18 subjects per group will be assigned at study start. Drop-outs will not be replaced during the study.
The primary parameter is the difference of plaque index between baseline (V1) value and the value after 12 weeks +/- 5 days (V3) of product use. For primary statistical analysis, a t-tests (unpaired situation) will be performed at a one-sided significance level of α=0.05. The primary efficacy analysis will be performed on the ITT-analysis set.
Secondary variables will be assessed with t-tests and confidence intervals to compare differences between V2, V3, and baseline for test product group and negative control group. Descriptive statistics will be performed for oral examinations for each group (counts and percentages of scores for nominal and ordinal scaled data, for at least ordinal scaled data minimum, maximum, median, mean value and standard deviation).
A two-sided significance level of α=0.05 is chosen for all secondary analyses, no adjustment for multiplicity will be done. Safety assessments will be based mainly on the frequency of adverse events.
Typ studiów
Zapisy (Rzeczywisty)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Lokalizacje studiów
-
-
-
Dresden, Niemcy, 01307
- Technische Universität Dresden
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Male and female adults (aged 18 to 65 years),
- Individuals with gingival inflammation, mean full-mouth GI ≥ 1.2 at inclusion,
- Individuals with plaque, mean full-mouth PI ≥ 1.2 at inclusion,
- Non-smokers or former smokers for at least 1 year or occasional smokers with a maximum of 5 cigarettes per week,
- Individuals who have at least 20 own teeth excluding the wisdom teeth,
- Subjects must have read, understood and signed the informed consent form
- Willingness to abstain from use of interdental brushing devices that contain antibacterial agents, like amine fluoride, chlorhexidine, silver ions etc. during the full course of the study
Exclusion Criteria:
- Individuals who have severe systemic diseases (tumors, infectious diseases) and diseases that require regular systemic medication intake that may affect the gingival condition (e. g. phenytoin, nifedipine, cyclosporine, antibiotics, steroids, antiphlogistics)
- Individuals who have moderate and severe chronic or aggressive periodontitis (PSI > 2 in more than 2 sextants or PSI > 3),
- Individuals who require antibiotic treatments for dental appointments (endocarditis prophylaxis), Individuals treated with antibiotics less than 8 weeks prior to the baseline examination and/or during the duration of the trial,
- Individuals who have participated in another clinical study less than 4 weeks prior to the baseline examination,
- Individuals who have mucosal diseases,
- Individuals who have severe oro-pharyngeal infections,
- Individuals who have significant dental disorders (e.g.: caries, suspected pulp pathology, abscess, pulpitis),
- History of gingival surgery in the previous three month,
- Ongoing dental treatment or any other medical treatment of the oral cavity,
- Individuals who are pregnant or breast feeding,
- Individuals with a history of chronic drug abuse or another illness which does not allow the person to assess the nature and/or possible consequences of the study,
- Smokers with more than 5 cigarettes per week,
- Individuals with known hypersensitivity or allergy to the test products and its ingredients,
- Individuals who were treated with antibacterial mouthrinses (e. g. chlorhexidine) 4 weeks or less before recruitment,
- Individuals unwilling to abstain from additional oral hygiene measures during the treatment phase with exception of their habitual mechanical cleaning procedures,
- Non-Caucasians,
- Subjects can be excluded at the principal investigators discretion.
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Potroić
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: Test group
Amine fluoride toothpaste
|
toothpaste
|
|
Komparator placebo: Control group
Placebo Sodium monofluorophosphate toothpaste
|
toothpaste
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Plaque index (Silness and Loe 1964)
Ramy czasowe: Change in plaque index from baseline at 12 weeks
|
Difference of plaque index, compared between test group and control group.
|
Change in plaque index from baseline at 12 weeks
|
Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
|
Plaque index (Silness and Loe 1964)
Ramy czasowe: Change in plaque index from baseline at 3 weeks
|
Difference of plaque index, compared between test group and control group.
|
Change in plaque index from baseline at 3 weeks
|
|
Plaque index (Silness and Loe 1964)
Ramy czasowe: Change in plaque index from week 3 at 12 weeks
|
Difference of plaque index, compared between test group and control group.
|
Change in plaque index from week 3 at 12 weeks
|
|
Gingival Index (Loe 1967)
Ramy czasowe: Change in gingival index from baseline at 3 weeks
|
Difference of gingival index, compared between test group and control group.
|
Change in gingival index from baseline at 3 weeks
|
|
Gingival Index (Loe 1967)
Ramy czasowe: Change in gingival index from baseline at 12 weeks
|
Difference of gingival index, compared between test group and control group.
|
Change in gingival index from baseline at 12 weeks
|
|
Gingival Index (Loe 1967)
Ramy czasowe: Change in gingival index from 3 weeks at week 12
|
Difference of gingival index, compared between test group and control group.
|
Change in gingival index from 3 weeks at week 12
|
|
Modified Sulcus Bleeding Index (Muhlemann and Son 1971):
Ramy czasowe: Change in bleeding index from baseline at 12 weeks
|
Difference of bleeding index, compared between test group and control group.
|
Change in bleeding index from baseline at 12 weeks
|
|
Modified Sulcus Bleeding Index (Muhlemann and Son 1971):
Ramy czasowe: Change in bleeding index from baseline at week 3
|
Difference of bleeding index, compared between test group and control group.
|
Change in bleeding index from baseline at week 3
|
|
Modified Sulcus Bleeding Index (Muhlemann and Son 1971):
Ramy czasowe: Change in bleeding index from week 3 at week 12
|
Difference of bleeding index, compared between test group and control group.
|
Change in bleeding index from week 3 at week 12
|
|
Adverse events
Ramy czasowe: up to 12 weeks from baseline
|
List all
|
up to 12 weeks from baseline
|
Współpracownicy i badacze
Sponsor
Współpracownicy
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów
Zakończenie podstawowe (Rzeczywisty)
Ukończenie studiów (Rzeczywisty)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Oszacować)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Oszacować)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- PAR012015
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .