The Influence of Anatomical Characteristics and Orthodontic Force on Pulpal Oxygen Saturation: A Clinical Study Using Cone-Beam Computed Tomography (CBCT)
The primary objective of this clinical protocol is to evaluate and compare the physiological responses of dental pulp to two different magnitudes of orthodontic force during active orthodontic treatment. Participants are assigned to either a 150g orthodontic force group (experimental group) or a 50g orthodontic force group (active comparator group).
Orthodontic Force Application: A continuous orthodontic force of approximately 150g is applied to the target teeth in the experimental group, whereas a continuous force of approximately 50g is applied to the target teeth in the active comparator group. The magnitude of the applied force is verified using a tension gauge to ensure standardized force delivery.
Pulse Oximetry (SpO₂) Measurement: Pulp oxygen saturation (SpO₂) is assessed using the same standardized protocol in both groups. The target teeth are isolated with cotton rolls to control moisture, and the dental chair light is turned off to minimize optical interference with the pulse oximeter. Three consecutive measurements are obtained at each assessment time point, and the mean value is recorded for analysis.
This standardized protocol enables comparison of pulp oxygen saturation responses between teeth subjected to 150g and 50g orthodontic forces while minimizing variability related to force application and measurement procedures.
調査の概要
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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Can Tho、ベトナム、900000
- Can Tho University of Medicine and Pharmacy
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参加基準
適格基準
就学可能な年齢
- 子
- 大人
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Patients aged between 15 and 35 years old.
- Patients undergoing routine fixed orthodontic treatment with indications for premolar extractions and subsequent canine retraction phase.
- Target canines must be vital with healthy dental pulp and no periapical pathology.
- Pre-existing Cone-Beam Computed Tomography (CBCT) scans of acceptable diagnostic quality available in the patient's records, taken prior to the canine retraction phase.
- Patient or legal guardian provides written informed consent to participate in the study.
Exclusion Criteria:
- Target canines with a history of dental trauma, extensive caries, periodontal disease, or previous endodontic treatment.
- Patients with systemic diseases affecting peripheral blood circulation or microvasculature (e.g., cardiovascular diseases, severe anemia, diabetes, chronic respiratory conditions).
- Patients currently using systemic vasoconstrictors or anti-inflammatory medications during the active monitoring period.
- Pregnancy or lactation.
- Refusal to sign the informed consent form.
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：診断
- 割り当て：ランダム化
- 介入モデル：クロスオーバー割り当て
- 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 |
|---|---|
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実験的：150g Orthodontic Force Group
Participants in this group receive a controlled orthodontic force of approximately 150 g applied to the target teeth.
The applied force is verified using a tension gauge.
Pulp oxygen saturation (SpO₂) is assessed at predefined time points.
At each assessment, three consecutive measurements are obtained under moisture isolation with the dental chair light turned off to minimize optical interference, and the mean SpO₂ value is recorded.
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A controlled mechanical orthodontic force of approximately 150g is applied to the target teeth and verified using a tension gauge.
The force is applied to induce orthodontic tooth movement, and pulp oxygen saturation (SpO₂) is monitored at predefined follow-up time points.
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アクティブコンパレータ：50g Orthodontic Force Group
Participants in this group receive a controlled orthodontic force of approximately 50 g applied to the target teeth.
The applied force is verified using a tension gauge.
Pulp oxygen saturation (SpO₂) is assessed at the same predefined time points and using the same standardized measurement protocol as in the 150-g group.
Three consecutive measurements are obtained at each assessment, and the mean SpO₂ value is recorded.
|
A controlled mechanical orthodontic force of approximately 50g is applied to the target teeth and verified using a tension gauge.
The force serves as the active comparator, and pulp oxygen saturation (SpO₂) is monitored at the same predefined follow-up time points as in the 150g group.
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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 |
|---|---|---|
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Changes in Dental Pulp Oxygen Saturation (SpO2) Levels
時間枠：Baseline (pre-force), 20 minutes, 24 hours, 7 days, and 4 weeks post-force application
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Dental pulp oxygen saturation levels are measured in percentages (%) using a customized pulse oximeter probe adapted for dental use.
The objective is to evaluate the physiological microcirculatory response of the canine pulp following orthodontic force application.
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Baseline (pre-force), 20 minutes, 24 hours, 7 days, and 4 weeks post-force application
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Alveolar Bone and Root Anatomical Measurements on CBCT
時間枠：Baseline (at the time of the pre-existing CBCT scan prior to the canine retraction phase)
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Three-dimensional anatomical variables are measured secondarily from pre-existing Cone-Beam Computed Tomography (CBCT) scans using specialized imaging software.
Variables include cortical bone thickness (mm) at the canine apex region, root apex-to-cortical plate distance (mm), and total root length (mm).
These baseline metrics will be correlated with the observed SpO2 changes.
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Baseline (at the time of the pre-existing CBCT scan prior to the canine retraction phase)
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協力者と研究者
捜査官
- 主任研究者：Lam Nguyen Le, Assoc. Prof.、Faculty of Odonto-Stomatology, Can Tho University of Medicine and Pharmacy
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
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
本研究に関する用語
キーワード
その他の研究ID番号
- Prof. Le Nguyen Lam
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
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