A RANDOMIZED COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFECT OF PASHUPATA VARTI ANJANA AND PASHUPATA EYE DROPS IN ABHISHYANDA W.S.R. TO CONJUNCTIVITIS.
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
研究概览
简要总结
This randomized comparative clinical trial is designed to evaluate and compare the safety and therapeutic efficacy of Pashupata Varti Anjana and Pashupata Eye Drops in the management of Abhishyanda, which is correlated with conjunctivitis in modern medicine. Abhishyanda is characterized by symptoms such as redness, itching, discharge, burning sensation, and irritation of the eyes. A total of 100 participants diagnosed with Abhishyanda will be randomly allocated into two groups. One group will receive Pashupata Varti Anjana, while the other group will receive Pashupata Eye Drops for a duration of 7 days. Clinical assessment will be done based on subjective symptoms and objective ophthalmological findings before and after treatment. The objective of the study is to scientifically evaluate and compare the effectiveness, safety, and patient acceptability of the traditional Anjana form and the modified eye drop form of Pashupata formulation. The study aims to provide clinical evidence for the use of Ayurvedic formulations as a safe and effective treatment option for conjunctivitis.
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
- 18.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •Participants between the age group of 18-60 years will be selected irrespective of gender.
- •Participants fulfilling one or more features of conjunctivitis.
排除标准
- •Participants with keratoconjunctivitis, giant papillary conjunctivitis.
- •Known case of glaucoma.
- •Participants who have undergone eye surgery within last 6 months and suffering from corneal pathology, ocular injuries and suspected foreign body in the eye.
- •Participants taking anti allergic medication and also using any kind of eye drops.
- •Pregnant ladies and lactating mothers.
研究者
Dr Sumi S
Parul Institue of Ayurved and Research
