Efficacy and Safety of Modified ORS(Amr and Khulood ORS) in Diabetic Pilgrims During Hajj (AA-HAMS-ORS)
Efficacy and Safety of Modified Oral Rehydration Salts (ORS) in Diabetic Pilgrims With Heat Stress and Dehydration During the Hajj Mass Gathering: A Three-Arm, Active-Controlled, Randomized Clinical Trial
調査の概要
状態
詳細な説明
Background: The Hajj pilgrimage involves strenuous physical activity in extreme heat, posing a high risk of dehydration and heat-related illnesses, particularly for diabetic patients. Standard ORS, while lifesaving, contains glucose that can exacerbate hyperglycemia.
Objective: To assess whether a modified ORS (Amr and khulood ORS) (with reduced or alternative carbohydrate sources) can safely and effectively rehydrate diabetic pilgrims.
Methods: This is a prospective, randomized, double-blind controlled trial. Participants will be diabetic pilgrims presenting with signs of mild to moderate dehydration. They will be randomized to receive either the modified ORS ( Amr and khulood ORS) or the WHO standard ORS.
Measurements: Blood glucose levels, serum electrolytes, urine specific gravity, and clinical signs of rehydration will be monitored at baseline and at regular intervals (2, 4, and 6 hours) post-intervention.
Safety: Adverse events, including severe hyperglycemia or hypoglycemia, will be recorded.
Significance: If proven effective, the modified ORS ( Amr and khulood ORS) could become a standard of care for diabetic individuals in heat-intensive environments, improving safety and health outcomes during Hajj.
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：amr Central Research Office
- 電話番号：+966597310032
- メール：amrka@moh.gov.sa
研究場所
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Riyadh、サウジアラビア
- Ministry of health
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コンタクト：
- Principal Investigator
- 電話番号：+966597310032
- メール：drmedahmed@gmail.com
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Diabetic pilgrims attending Hajj.
- Age between 18 and 80 years.
- Willingness to participate and provide informed consent.
- Diagnosis of Type 1 or Type 2 Diabetes Mellitus.
Exclusion Criteria:
- Patients with severe renal failure.
- Patients with acute cardiovascular events.
- Patients unable to take oral fluids.
- Pregnancy or breastfeeding.
- Participation in another clinical trial within the last 30 days.
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：トリプル
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：Modified ORS Group
Participants in this group will receive the modified Oral Rehydration Salts ( Amr and khulood ORS) specifically designed for diabetic patients during the Hajj season to prevent dehydration and maintain electrolyte balance.
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Modified ORS formula ( Amr and khulood ORS) with adjusted electrolyte and carbohydrate content suitable for diabetic patients to prevent heat-related dehydration.
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アクティブコンパレータ：Standard ORS Group
Participants in this group will receive the standard World Health Organization (WHO) Oral Rehydration Salts (ORS) formula.
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Standard World Health Organization (WHO) ORS formula used as an active comparator.
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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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Change in serum sodium levels from baseline to post-treatment
時間枠：Baseline and 24 hours post-treatment
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Assessment of electrolyte balance by measuring the change in serum sodium levels (mmol/L) after the administration of ORS.
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Baseline and 24 hours post-treatment
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協力者と研究者
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
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