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临床试验/CTRI/2025/05/086523
CTRI/2025/05/086523尚未招募3 期

Randomised control clinical trial to evaluate the efficacy of haritakyadi varti anjana in kaphaj abhishyanda with special referance to acute mucopurulent conjunctivitis.

Dipali Dilip Rupnar1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年5月20日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
To study the effect of Haritakyadi varti anjana in the management of Kaphaj Abhishyanda.

研究概览

简要总结

Aim - To evaluate the efficacy of Haritakyadi Varti Anjana in Kaphaj Abhishyanda with special referance to Acute Mucopurulent Conjunctivitis.

Primary Objective - To study efficacy of Hritakyadi Varti Anjana in Kaphaj Abhishyanda with special referance acute mucopurulent conjunctivitis.

Secondary Objective -   To study the detail literature about Kaphaj Abhishyanda.

To study the detail literature about acute mucopurulent conjunctivitis

To study the effect of Haritakyadi Varti Anjana in Kaphaj Abhishyanda with special referance to Acute Mucopurulent Conjunctivitis.

Type of study design -    Double Arm Clinical Study , Open study

Study setting -  Patients having symptoms related to Kaphaj Abhishyanda will be registered from the Shalakya OPD in our hospital.

Study Population -  80

Duration of Treatment - 5 Days

Overall Duration of Study - 18 months

Follow up - 1st, 3rd, 5th, 7th, 15th Day

Diagnostic criteria -

Patients will be diagnosed on the basis of clinical signs and symptoms.

Assessment Criteria -

Subjective parameters are based on symptomatic relief i.e - Netra Kandu , Photophobia

The data obtained will be analyzed statistically.

Observation and Result -   The obtained Clinical efficacy of treatment will be observed and recorded.

Discussion -  On the basis of collection of data discussion will be done

Conclussion  -  Conclussion will be done on the basis of  statistical significant i.e as per obtained result and observation the clinical study will be discussed.

Summary - The research study will be summarized in brief.

Ethical consideration - The study will be conducted in accordance with ethical guidelines and inform concent from participants.

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

年龄范围
16.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • 1.Patients showing classical sign and symptoms of Kaphaj Netra Abhishyanda 2.Patients irrespective of sex, occupation and socio economic status will be selected.

排除标准

  • 1.Patients of age group below 16 years and above 50 years 2.Patients with other ocular diseases 3.Recently eye operated patients 4.Patients with other major systemic diseases 5.Using any other eye medication 6.Patients with sever complaints will exclude.

结局指标

主要结局

To study the effect of Haritakyadi varti anjana in the management of Kaphaj Abhishyanda.

时间窗: 15 days

次要结局

  • 1.To study the detail literature about Kaphaj Abhishyanda(2.To study the detail literature about Acute Mucopurulent Conjunctivitis.)

研究者

发起方
Dipali Dilip Rupnar
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dipali Dilip Rupnar

LRP Ayurved Medical College and Hospital,Post Graduate Institute and Reasearch Centre,Islampur.

研究点 (1)

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