A study on the impact of intraoperative Intravitreal Triamcinolone Acetonide injection on visual outcome, postoperative complications and visual rehabilitation in patients of uveitic cataract undergoing SICS
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- 1 visual acuity
研究概览
简要总结
it is a randomized prospective interventional study. it will be conducted at a tertiary eye care center over a year with a sample size of 30 patients. The study aims to compare the outcome of uveitic cataract patients undergoing small incision cataract surgery with and without a 3mg intravitreal triamcinolone acetonide injection, focusing on visual outcomes, complications, and rehabilitation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 19.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Inclusion Criteria: 1.Diagnosis of uveitis consistent with Standardization Uveitis Nomenclature (SUN).
- •2.Intraocular inflammation had been controlled without using topical or oral corticosteroid for atleast 3 months before surgery .
排除标准
- •Exclusion Criteria : 1.Infectious uveitis.
- •Previous intraocular surgery .
- •3.Patients with history of glaucoma or high myopia, optic neuropathy, media opacity other than cataract .
- •4.Patients less than 18 years or with juvenile rheumatoid arthritis.
- •5.Retinal or choroidal disease.
- •6.Intraoperative posterior capsular rupture or viterous loss.
结局指标
主要结局
1 visual acuity
时间窗: postoperative day 1 | 1 week | 1 month | 2 months | 3 months | 6 months
2 Intraocular pressure
时间窗: postoperative day 1 | 1 week | 1 month | 2 months | 3 months | 6 months
3 central Macular Thickness
时间窗: postoperative day 1 | 1 week | 1 month | 2 months | 3 months | 6 months
4 Anterior Chamber reaction
时间窗: postoperative day 1 | 1 week | 1 month | 2 months | 3 months | 6 months
5 endothelial cell density
时间窗: postoperative day 1 | 1 week | 1 month | 2 months | 3 months | 6 months
次要结局
- postoperative complications(postoperative day 1)
研究者
MIRZA MARIYAM BEG
Moti Lal Nehru Medical college