Hydrolyzed Collagen As A Host Modulation Agent in Non-Surgical Periodontal Treatment
Investigation of the Host Modulator Efficacy of Food Supplement Containing Hydrolyzed Collagen in Non-Surgical Periodontal Treatment of Patients With Periodontitis
This study was planned on the basis of the hypothesis that 'food supplements containing collagen will support the clinical effectiveness of non-surgical periodontal therapy'. In this context, the aim of the study is to investigate the therapeutic efficacy of collagen-containing food supplement as a host modulation agent in the non-surgical periodontal treatment of individuals with stage 3-4 periodontitis in a clinical and biochemical manner in a comprehensive manner.
Initial day: Anamnesis, diagnosis and index measurements 2 days later, collection of serum samples from the patient, oral hygiene training and straightening of the whole mouth root surface and cleaning of the whole mouth tooth surface The next day, full mouth scalling and root planing are closed with the second session and tablets are started.
End of 2nd month:
Periodontal index measurement and oral hygiene training Collecting serum and tissue samples 2 days later
End of 6th month Periodontal index measurement and oral hygiene training Collecting serum and tissue samples 2 days later
調査の概要
状態
条件
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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Rize Province
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Rize、Rize Province、トルコ(Türkiye)、53000
- Recep Tayyip Erdogan University
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参加基準
適格基準
就学可能な年齢
- 大人
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- 18 - 60 age
- stage 3-4 periodontitis
Exclusion Criteria:
- Patients who smoke more than 10 cigarettes a day
- Patients using immunosuppressive, oral contraceptive, bisphosphonate drugs
- Patients who are during pregnancy or lactation
- Having undergone periodontal treatment in the last 6 months, having used antibiotic anti-inflammatory medication in the last 4 weeks
- The presence of any autoimmune disease, osteoporotic disease or cancer disease
- Patients with renal and hepatic insufficiency
- Patients with thyroid dysfunction
- The presence of active infectious diseases(acute hepatitis, tuberculosis, AIDS)
- Chronic drug use affecting periodontal tissues(cyclosporine A, Phenytoin)
- Intake of antioxidant supplements
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:支持療法
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
プラセボコンパレーター:プラセボ群
|
placebo will be given.
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アクティブコンパレータ:Patients using collagen peptides
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Collagen supplements will not be given in the placebo 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 |
|---|---|---|
|
probing pocket depth
時間枠:baseline, 1st month and 3rd month
|
The distance between the gingival margin and the pocket base was measured in millimeters.
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baseline, 1st month and 3rd month
|
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clinical attachment loss
時間枠:baseline, 1st month and 3th month
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The distance from the enamel-cementum junction to the pocket base was measured in millimeters.
|
baseline, 1st month and 3th month
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
assessment of interleukin-1 beta levels
時間枠:baseline, 1st month and 3th month
|
Serum interleukin-1 beta levels were measured biochemically.
|
baseline, 1st month and 3th month
|
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assessment of matrix metalloproteinase-8 (MMP-8) levels
時間枠:baseline, 1st month and 3 th month
|
Matrix metalloproteinase-8 (MMP-8) levels in gingival crevicular fluid were measured biochemically.
|
baseline, 1st month and 3 th month
|
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 (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
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。