Esthetic Impact of Different Minimally Invasive Approaches on Hypomineralized Permanent Anterior Teeth
Esthetic Impact of Different Minimally Invasive Approaches on Hypomineralized Permanent Anterior Teeth: A Randomized Clinical Trial
The aim of the study is to determine the effectiveness of minimally invasive treatments in reducing the visible enamel opacities on permanent anterior teeth in children aged from seven to twelve years with hypomineralized lesions.
A secondary purpose is to evaluate patient satisfaction and the psychosocial impact of the treatment on the esthetic perception of the treated children.
The results of all the research papers about treating enamel discoloration caused by hypomineralization with the ICON system can be accepted as satisfactory. However, not all cases achieved the full aesthetic aim.
Microabrasion is an acid abrasive removal and not the dissolution of enamel stain. It is as a treatment modality for enamel opacities like brown, orange, or yellow enamel spots; and fluorotic white streaks. Esthetic results could be reached when microabrasion followed by a remineralizing agent such as C PP-ACFP.
Null hypothesis, there is no difference between microabrasion followed by a remineralizing agent and resin infiltration treatment regarding clinical effectiveness & patient satisfaction.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
Outcomes:
Primary outcome Color enhancement using Clinical photographs (Bhandari, et al., 2019). Secondary outcomes
- Patient satisfaction will be evaluated using Numerical scale (NS), (Figure 1). The participant marked the number that represented their self-assessed satisfaction (Rocha et al., 2020) as shown in Appenxix II.
- Psychosocial impact of the treatment on the esthetic perception of the treated children will be evaluated using The Psychosocial Impact of Dental Aesthetics Questionnaire (PIDAQ) (Klages et al., 2006). Appendix III.
- Reducing teeth hypersensitivity will be evaluated using The Schiff Cold Air Sensitivity Scale (SCASS) (Schiff et al., 1994).
- Adverse and undesirable side effects experienced by the respondents: a) pain in teeth and gums will be evaluated using The Wong-Baker FACES® Pain Rating Scale (Wong et al., 1988). Appendix IV.
- b) bitter taste will be evaluated by asking the child right after treatment. (Athayde et al., 2022).
- Follow up:
Follow up after 1 day for adverse and undesirable side effects, 1week & 6 months.
Randomization:
The participants will be randomly assigned to one of the three experimental groups the interventions and control groups using simple randomization with a 1:1 allocation ratio.
Masking/blinding:
Neither the operator nor the patients could be blinded due to the nature of the study but the outcome assessor and statistician will be blinded.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- 適用できない
連絡先と場所
研究連絡先
研究連絡先
- 名前:Shaimaa AM Awad, Mcs
- 電話番号:01027557531
- メール:shaimaa.awad@dentistry.cu.edu.eg
研究連絡先のバックアップ
- 名前:Aliaa AM Awad
- 電話番号:01062811856
- メール:shaimaa.awad@dentistry.cu.edu.eg
研究場所
-
-
-
Cairo、エジプト
- Faculty of Dentistry, Cairo University
-
コンタクト:
- Shaimaa Awad, Mcs
- 電話番号:01027557531
- メール:shaimaa.awad@dentistry.cu.edu.eg
-
-
参加基準
適格基準
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:
-
▪ Participants free from any systemic disease aged from 7 years to 12 years
- Anterior permanent teeth with Degree 1(mild) hypomineralization (according to the Wetzel and Reckel scale) (as shown in Appenxix I).
- Enamel opacities, (White, creamy or yellow to brownish colour), without enamel breakdown
- Caries-free teeth.
- Sensitivity to external stimuli e.g., air/water but not brushing.
Exclusion Criteria:
-
▪ Dental caries and filling,
- Loss of the enamel or dentin structure,
- Clinical symptoms of irreversible pulpitis such as spontaneous pain or persisting pain,
- Previous use of bleaching agent.
- Dental anomaly on anterior teeth,
- Periodontal diseases,
- Undergoing orthodontic treatment,
- Cognitive and behavioral conditions.
- Patients with milk protein or hydroxybenzoates allergies.
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:処理
- 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
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
アクティブコンパレータ:Control group ICON® resin infiltration
Resin infiltration treatment (Icon®) for Hypomineralized anterior permanent teeth in children |
|
|
実験的:Intervention group 1
Opalustre® Enamel Microabrasion Slurry |
NOTE: For hypo-mineralization greater than 0.1-0.3mm use a fine-grit water-cooled tapered diamond bur, lightly sweep over the stained area for 5-10 seconds prior to applying Opalustre.
|
|
実験的:Intervention group 2
Antivet® enamel micro-abrasion |
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Color enhancement measured by Clinical photographs
時間枠:6 months
|
Clinical photographs will be taken with a digital camera macro lens, and flash. With the patient and digital camera at the same vertical plane and dental clinic illuminated evenly. The photographs will be taken in baseline, during the application time of the test or control. For standardizing the photographic conditions, the camera will be placed at the equidistance from the tooth. To prevent the change of refractive index by moisture, 30 s of drying of the lesion will be done. |
6 months
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Patient satisfaction measured by Visual analogue scale
時間枠:6 months
|
The patient is asked to draw a line perpendicular to the VAS at their perceived pain-intensity level, no discomfort (score 0), mild discomfort (score 1-3), moderate (score 4-6) and very severe (7-9) or worst discomfort (score 10). |
6 months
|
|
Reducing teeth hypersensitivity measured by The Schiff Cold Air Sensitivity Scale (SCASS)
時間枠:6 months
|
It is a behavioral scale because it is based on observed behavior in response to a stimulus beyond a certain threshold. The dentist (or another assessor present) rates the response of the patient to the stimulus as 0 for no response to air stimulus,
|
6 months
|
協力者と研究者
捜査官
捜査官
- 主任研究者:Shaimaa AM Awad, Mcs、Cairo Uviversity
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- 261711198415920202321948291954
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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。