Comparative clinical study to evaluate the efficacy of nayansukhavarti anjana and rasanjana in prastari arma with special reference to progressive pterygium
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 82
- 试验地点
- 1
- 主要终点
- To evaluate the efficacy of nayansukhavarti anjana and rasanjana in prastari Arma
研究概览
简要总结
As we see the number of patients with Prastari Arma increasing now a days so this study will help the patients to relieve the symptoms by the exertion of Doshas and cheaper than surgical treatment and easily available this study is comparitve clinical open trial The efficacy of Nayansukhavarti Anjana and Rasanjana will be compared in the mangement of Prastari Arma with special reference to Progressive Pterygium 41 patients will be selected in each group Group A patients will be treated with Nayansukhavarti Anjana and Group B will be trated with Rasanjana Procedure will be done once in a day for 15 days follow up will be done on with treatment 7th 14th and without treatment 21th 30th days Study will be conducted in India outcome of study will be assessed on basis of Slit Lamp examination and Castroviejo Caliper and reduction of signs and symptoms of Progressive Pterygium will be noted
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Open Label
入排标准
- 年龄范围
- 30.00 Year(s) 至 70.00 Year(s)（—）
入选标准
- •1 Patient which shows sign and symptoms of Prastari Arma 2 Pterygium, both from inner and outer canthus 3 Pterygium limited to scleral part (up to Limbus) only 4 Patient irrespective of Gender educational status socio economical status marital statuscaste Religion Race etc.
排除标准
- •1 Any acute infective ocular disease 2 Recently operated eye 3 Pterygium encroaching cornea 4 Patient having major complicated systemic and eye disease.
结局指标
主要结局
To evaluate the efficacy of nayansukhavarti anjana and rasanjana in prastari Arma
时间窗: 4 weeks
次要结局
- To compare the efficacy of nayansukhavarti anjana & rasanjana in prastari Arma(4 weeks)