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临床试验/CTRI/2025/09/094719
CTRI/2025/09/094719尚未招募2 期

Comparative Clinical Evaluation of Shaivaladi Tail Karnapichu and Samudraphena Avachurnan in Karnasrava(Tubo-tympanic type of CSOM)

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan. Haridwar1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年9月27日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1. Ear Discharge

研究概览

简要总结

In this trial, we are selecting the patients of Karnasrava in which we will do the intervention in 2 groups - 30 patients in each group. In one group, we will intervene with ayurvedic therapeutic procedure of karnapichu with shaivaladi tail once daily in two sittings of 7-7 days with 7 days gap in between, whereas in other group we will intervene with another ayurvedic therapeutic procedure of avachurnan with Samudraphena once daily in two sittings of 7-7 days with 7 days gap in between. First follow-up will be on 15th day after the completion of treatment and second follow-up will be after 15 days of first follow-up. Assessment will be done on the basis of subjective and objectives parameters and scoring will be done before and after the treatment.

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
10.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients with age group of 10 years to 70 years.
  • Patients presenting with sign and symptoms of Tubo tympanic type of CSOM.
  • Patient willing to participate in this trial through written consent.

排除标准

  • Patients below 10 years and above 70 years of age.
  • Pregnant women and lactating mothers.
  • Patient suffering with systemic diseases like Diabetes Mellitus (Type I and II ), Meningitis, Tuberculosis.
  • Patients with Attico antral type of CSOM .
  • Patients with the complications of CSOM like Mastoiditis, Subdural Abscess,Extradural Abscess , Labyrinthitis, Vertigo .
  • Patients with Otomycosis.

结局指标

主要结局

1. Ear Discharge

时间窗: 0,3 weeks ,6 weeks,8 weeks

2. Pain in ear

时间窗: 0,3 weeks ,6 weeks,8 weeks

3. Itching in ear

时间窗: 0,3 weeks ,6 weeks,8 weeks

4. Tinnitus

时间窗: 0,3 weeks ,6 weeks,8 weeks

次要结局

  • Objective parameter will be assessed-(1. Hearing loss)

研究者

发起方
Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan. Haridwar
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Charvi Verma

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan

研究点 (1)

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