CTRI/2023/03/050981尚未招募不适用
TO STUDY THE ROLE OF SUPRACHOROIDAL INJECTION TRIAMCINOLONE IN NON-INFECTIOUS UVEITIS
GSVM MEDICAL COLLEGE1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年3月27日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- 1) BCVA
研究概览
简要总结
This is Randomised prospective study , to assess the role of suprachoroidal injection of Triamcinolone in patients of non- infectious anterior, non-infectious intermediate and non-infectious posterior uveitis. Primary outcome will be BCVA improvement in 3-15 days.
研究设计
- 研究类型
- Interventional
- 分配方式
- Adaptive randomization, such as minimization
- 盲法
- Open Label
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Newly diagnosed patients of non-infectious anterior uveitis.
- •(2) Newly diagnosed patients of non-infectious intermediate uveitis.
- •(3) Newly diagnosed patients of non-infectious posterior uveitis.
排除标准
- •(1) Patients not willing to participate or ready for follow up.
- •(2) Patients with uncontrolled blood sugar.
- •(3) Patients with any ocular disease other than uveitis.
- •(4) Patients contraindicated for suprachoroidal injection eg.
- •thinned sclera, scleritis, staphylococcus.
- •(5) Patients of hypersensitivity for Triamcinolone.
- •(6) Patients diagnosed of any other posterior segment pathologies.
结局指标
主要结局
1) BCVA
时间窗: 3 days after injection
2) Slit lamp examination
时间窗: 3 days after injection
3) Intra ocular pressure
时间窗: 3 days after injection
次要结局
- BCVA(Slit lamp examination)
研究者
研究点 (1)
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