跳至主要内容
临床试验/CTRI/2022/07/044372
CTRI/2022/07/044372尚未招募4 期

Camparative Evaluation of Manjishtadi Taila and Mahamasha Taila Nasya in the Management of Avabahuka (Frozen Shoulder).

Dr Kanchan R Sorte1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年1月8日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
We will see the imapct of nasya in Avabahuka on subjective parameters during treatment.It is hypothesized that Mahamasha taila nasya and Manjishthadi taila nasya will be more effective with no adverse effect.

研究概览

简要总结

Patients will be recruited from inclusion criteria and study the efficacy of Manjisthadi taila and Mahamash taila nasya in Avabahuka

To study the efficacy of Manjisthadi taila Nasya in Avabahuka.

To study the efficacy of Mahamash taila Nasya in Avabahuka

Comparative evaluation of the efficacy of Manjisthadi taila and mahamash taila nasya in avabahuka.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Open Label

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Avabahuka is diagnosed according to the classical sign and symptoms include restricted movement and pain in the affected shoulder, stiffness and muscle wasting 2) Patients of either sex between the age group of 18-60 years 3) Patients fit for Nasya Karma.
  • Patients are ready to give consent and abide by the study protocol.

排除标准

  • Patients complaining of fracture and dislocation.
  • patients with a history of Hemorrhagic Hemiplegia.
  • Patients having nasal disorders.
  • Patients having diabetes.

结局指标

主要结局

We will see the imapct of nasya in Avabahuka on subjective parameters during treatment.It is hypothesized that Mahamasha taila nasya and Manjishthadi taila nasya will be more effective with no adverse effect.

时间窗: six months

次要结局

  • We will see the effect of Mahamasha taila nasya and Manjishthadi taila nasya on objective parameters by assessing range of motion.The secondary outcome is to compare the efficacy of Manjishthadi taila with mahamasha taila nasya in Avabahuka(Frozen shoulder)(Six months)

研究者

发起方
Dr Kanchan R Sorte
申办方类型
Other [self]

研究点 (1)

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