ACTRN12618001211257已完成未知
Determination of clinical factors that influence insulin dose requirements during treatment of hyperglycaemia while taking prednisolone
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •1. Age greater than or equal to 18 years
- •2. Prescribed a morning dose of oral prednisolone greater than or equal to 20 mg/day for an acute inflammatory illness.
- •3. Hyperglycaemia in the prior 24 hours, defined as:
- •A) One point-of-care blood glucose greater than or equal to 15 mmol/L.
- •B) Two point-of-care blood glucose greater than or equal to 10 mmol/L.
排除标准
- •1. by mouth or reduced oral intake.
- •2. Type 1 diabetes mellitus (T1DM).
- •3. Prescribed long-term oral prednisolone greater than or equal to 10 mg/day (or equivalent).
- •4. Psychiatric illness or another condition precluding providing informed consent.
- •5. Pregnancy.
研究者
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