Prospective Diabetes Registry of Patients With Type 2 Diabetes Mellitus on SGLT 2 Inhibitor Therapy in Singapore
SGLT2 Inhibitor Registry in Singapore
To evaluate clinical effectiveness and safety of Singaporean Type 2 Diabetes mellitus patients administered SGLT 2 inhibitor monotherapy or in combination with other commonly used hypoglycaemic drugs in real life clinical settings.
To evaluate real life clinical effectiveness and safety of Sodium-Glucose Co-Transporter inhibitor- 2 in Singaporean Type 2 diabetes mellitus patients treated on an outpatient basis in clinical practice setting. The study would also assess treatment patterns with SGLT2 inhibitor patient relevant outcomes in whole population as well as pre identified patient subgroups.
Primary analysis to be done at 1 year and extended analysis at 2 years.
調査の概要
状態
条件
詳細な説明
T2DM is associated with overweight/obesity and high fasting plasma glucose (FPG) in White patients, whereas Asian patients are more predisposed to high abdominal fat distribution and high postprandial glucose (PPG) levels, thought to contribute1-4. In response to identical meals, Asian subjects exhibit greater glycemic response than do White subjects4,5. According to the Diabetic Society of Singapore, one out of nine people aged 18 to 69 has diabetes, that's about 11.3% of the population or more than 400,000 people & this is expected to rise with the increasing prevalence of a sedentary lifestyle and high-calorie dietary intake.
SGLT2 inhibitors offers a novel insulin-independent approach to lowering hyperglycaemia and improving metabolic control of type 2 diabetes: they reduce renal glucose reabsorption by inhibition of SGLT2 transporters in the proximal tubule of the kidney, resulting in urinary glucose excretion. Since SGLT2 inhibition is independent of β-cell function or insulin sensitivity, this treatment approach could have applications throughout the natural history of diabetes.6
The reductions in fasting plasma glucose concentration and bodyweight during the treatment with the SGLT2 i, are sustained. Early weight loss, is partly due to a mild osmotic diuresis caused by SGLT2 I, however, the gradual progressive reduction in bodyweight thereafter, with decreased waist circumference, is consistent with a reduction of fat mass. This reduction is potentially attributable to the loss of excess energy through glucose excretion in the urine, an effect supported by the increased urinary glucose/creatinine ratio in patients assigned to SGLT2i.6
Many trials shows that SGLT2 i can improve glycaemic control in patients who have inadequate control with metformin. The drug acts independently of insulin, lowers weight, and is not associated with risk of hypoglycaemia. Safety and tolerability of the drugs were also confirmed. Therefore, addition of SGLT2i to metformin provides a new therapeutic option for treatment of type 2 diabetes.6
Data collection will be done by AZ medical personnel or Pharmacy interns, it will be a paper data collection and will be handed over to the CRO company for data entry & analysis..Data analysis will be done by an independent CRO company namely BioQuest Solutions.
研究の種類
入学 (実際)
連絡先と場所
研究場所
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Singapore、シンガポール
- Research Site
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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
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
Patients should meet all of the following criteria at Day 0:
- Outpatient equal to or more than 18 years of age
- Diagnosed as T2DM and treated with antidiabetic medicines at least 3 months and suitable for SGLT2 inhibitor as current treatment judged by PI with HbA1c > 7.0 %
- Will provide completed and signed written informed consents Each participating investigator, will be asked to recruit a fixed number of patients ranging from 10 to 40 depending on site specificities.
Exclusion Criteria:
Patients, with the following criteria will be excluded at Day 0:
- Hypersensitivity to any SGLT2 inhibitor or any of the components in the formulation
- Patients with Type 1 diabetes
- Female patients with gestational diabetes during pregnancy
- Female patients who are pregnant, intending to become pregnant or breastfeeding
- Severe medical condition(s) that in the view of the investigator prohibits participation in the study e.g. cancer, end stage liver disease, end stage renal failure (non-diabetes related)
- Use of other investigational drugs at the time of enrolment
- Renal Function: <30ml/min/1.73m2
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
- 観測モデル：ケースのみ
- 時間の展望：見込みのある
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 from baseline in the HbA1c level after 1 year
時間枠：baseline to 1 year
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to assess whether the therapy initiated with SGLT2 inhibitors at baseline is able to reduce the HbA1c after 1 year.
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baseline to 1 year
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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 |
|---|---|---|
|
Change from baseline in FPG level at 6months
時間枠：Blood samples are collected pre-dose, 6 months post-dose
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By assessment of the other lipid level reduction from baseline lab value to the last lab value
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Blood samples are collected pre-dose, 6 months post-dose
|
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Change from baseline in FPG level at 12months
時間枠：Blood samples are collected pre-dose, 12 months post-dose
|
By assessment of the other lipid level reduction from baseline lab value to the last lab value
|
Blood samples are collected pre-dose, 12 months post-dose
|
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Change from baseline in weight at 6months
時間枠：weight is measured pre-dose, 6 months post-dose
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By assessment of the other weight reduction from baseline value to the last value
|
weight is measured pre-dose, 6 months post-dose
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Change from baseline in weight at 12 months
時間枠：weight is measured pre-dose, 12 months post-dose
|
By assessment of the other weight reduction from baseline value to the last value
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weight is measured pre-dose, 12 months post-dose
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Change from baseline in BP at 6 months
時間枠：BP is measured pre-dose, 6 months post-dose
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By assessment of the other BP reduction from baseline value to the last value
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BP is measured pre-dose, 6 months post-dose
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Change from baseline in BP at 12 months
時間枠：BP is measured pre-dose, 12 months post-dose
|
By assessment of the other BP reduction from baseline value to the last value
|
BP is measured pre-dose, 12 months post-dose
|
|
Change from baseline in Lipids at 6 months
時間枠：Blood samples are collected pre-dose, 6 months post-dose
|
By assessment of the other lipid level reduction from baseline lab value to the last lab value
|
Blood samples are collected pre-dose, 6 months post-dose
|
|
Change from baseline in Lipids at 12 months
時間枠：Blood samples are collected pre-dose, 12 months post-dose
|
By assessment of the other lipid level reduction from baseline lab value to the last lab value
|
Blood samples are collected pre-dose, 12 months post-dose
|
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Change from baseline in Waist circumference at 6 months
時間枠：waist circumference is measured pre-dose, 6 months post-dose
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By assessment of the other waist circumference reduction from baseline value to the last value
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waist circumference is measured pre-dose, 6 months post-dose
|
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Change from baseline in Waist circumference at 12 months
時間枠：waist circumference is measured pre-dose, 12 months post-dose
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By assessment of the other waist circumference reduction from baseline value to the last value
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waist circumference is measured pre-dose, 12 months post-dose
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協力者と研究者
スポンサー
出版物と役立つリンク
一般刊行物
- REFERENCES 1. Wang JS, et al. Diabetes Metab Res Rev. 2011;27:79-84 2. Bonora E, et al. Diabetes Care. 2001;24:2023-2029 3. Peter R, et al. Diabet Med. 2006;23:990-995 4. Venn BS, et al. Diabet Med. 2010;27:1205-1208 5. Henry CJ, et al. Br J Nutr. 2008;99:840-845 6. Bailey CJ, et al. Lancet. 2010;375:2223-33
便利なリンク
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 (見積もり)
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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