Randomized controlled clinical trial to study the efficacy of triphala kwath sac syringing and normal saline sac syringing in management of chronic dacryocystitis.
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Sample size 50
研究概览
简要总结
The study will be intervened by the treatment of triphala kwath sac syringing and normal saline sac syringing to group A and group B respectively. The efficacy of the therapy will be assessed on the basis of subjective criteria for statistical analysis. Scoring will be designed according to the severity of symptoms. The subjective gradation of symptoms will be done as follows and the intensity of each symptom will be calculated before treatment, after treatment and after follow up. The effect of treatment result will be assessed in regards to clinical signs and symptoms on the basis of grading and scoring system. The signs and symptoms will be assessed by adopting the suitable scoring method.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 20.00 Year(s) 至 75.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients having symptoms of pain, swelling, watery discharge and congestion in eyes.
排除标准
- •Patients with acute infection in eyes.
- •Patients whose regurgitation test shows muco-purulent discharge.
- •Patients who have undergone cataract surgery within a month.
结局指标
主要结局
Sample size 50
时间窗: Sample size 50 | decrease in pain, congestion, watering and swelling of eyes.
decrease in pain, congestion, watering and swelling of eyes.
时间窗: Sample size 50 | decrease in pain, congestion, watering and swelling of eyes.
次要结局
- Sample size 50(decrease in pain, congestion, watering and swelling of eyes.)