Powered vs Manual Toothbrush Use: Its Effect on Caries Risk in Pre-Adolescents
Powered vs Manual Toothbrush Use: Its Effect on Caries Risk in Pre-Adolescents, A Pilot Study
This pilot study aims to evaluate dental caries experience in children ages 8-12 years old through comparing the use of a powered versus manual toothbrush, while using a standardized fluoride toothpaste as the control over the course of one year.
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Taylor Cezon, RDH
- 電話番号:734-730-8533
- メール:kidscavities@umich.edu
研究場所
-
-
Michigan
-
Ann Arbor、Michigan、アメリカ、48109
- 募集
- University of Michigan
-
主任研究者:
- Margherita Fontana, DDS, PhD
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
-
Child:
- Male OR Female, between 8 - 12 years old at baseline
- In good health (i.e., free of any medical condition that would reasonably be anticipated to interfere with study participation)
- Must allow examination of the oral cavity at baseline
- Must have at least an ICDAS 2 or higher at baseline or radiographic signs of untreated caries lesions E2 or higher, or caries experience in the last 3 years (extraction due to caries, restoration due to caries, etc.)
- Able to tolerate radiographs
- Able to brush teeth by themselves with no assistance
Parent/Legal Guardian:
- Provide written informed consent for the child and her/himself prior to participation
- Must be at least 18 years old, or an emancipated minor who provides documentation of emancipation
- Must be willing and able to participate in study activities
Exclusion Criteria:
-
Child:
- Hereditary generalized developmental dental defects such as Amelogenesis Imperfecta and Dentinogenesis Imperfecta
- Presence of pain, pulpal exposure, or signs of pulpal infection (abscess, fistula, swelling) at baseline
- Participating in the foster care system
- Demonstrated inability to comply with study protocol requirements (including radiographs or abstaining from using other oral hygiene products such as mouth rinses during the study period)
- Has removable OR fixed orthodontic appliances
- Participation (within 30 days of Baseline Visit) in any other oral hygiene clinical study
Parent/Legal Guardian:
• Demonstrated inability to comply with trial protocol requirements
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:防止
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
介入なし:Manual Toothbrush
|
|
|
実験的:Powered Toothbrush
|
Powered toothbrush Oral-B iO Kids Electric Toothbrush Featuring Stitch |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of new caries surfaces and number of progressed caries surfaces
時間枠:12 Months
|
Composite Endpoint. New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. Caries progression defined if baseline was enamel decay and follow-up was dentin decay, filling, or extracted due to caries. |
12 Months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of new caries surfaces
時間枠:12 Months
|
New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. |
12 Months
|
|
Number of new caries surfaces and number of progressed caries surfaces
時間枠:6 Months
|
Composite Endpoint. New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. Caries progression defined if baseline was enamel decay and follow-up was dentin decay, filling, or extracted due to caries. |
6 Months
|
|
Number of new caries surfaces
時間枠:6 Months
|
New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. |
6 Months
|
協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。