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临床试验/CTRI/2024/12/078683
CTRI/2024/12/078683尚未招募不适用

A clinical study to evaluate the effect of mahamasha taila greeva basti with partimarsha nasya in vishwachi w.s.r. to cervical spondylosis

未提供1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年1月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
30
试验地点
1
主要终点
Objective parameters

研究概览

简要总结

This is an open labelled study evaluating the efficacy of Mahamasha taila greeva basti  with Pratimarsha nasya which will be given for 7 days followed by 8 days of Pratimarsha nasya with mahamasha taila to 30 patients. The study will be conducted in Sri Dharamasthala Manjunatheshwara College of Ayurveda, Hospital and Research Centre, Kuthpady, Udupi. The primary outcome measures will be assessed by subjective and objective parameters. The secondary outcome measures will be assessed based on the quality of life scale. Hence this study is an effort to prove the efficacy of Mahamasha Taila Greeva Basti with Pratimarsha Nasya in Viswachi w.s.r to Cervical Spondylosis.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
20.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients fulfilling diagnostic criteria of cervical spondylosis
  • Patients fit for greeva basti and pratimarsha nasya.

排除标准

  • Patients with fracture of cervical spine
  • Patients suffering from neoplastic disorders
  • Patients with major systemic disorders that may interfere with course of treatment
  • Pregnant and lactating women.

结局指标

主要结局

Objective parameters

时间窗: 0th day, 7th day and 15th day

Neck disability index

时间窗: 0th day, 7th day and 15th day

Muscle power

时间窗: 0th day, 7th day and 15th day

Primary outcome will be assessed based on the

时间窗: 0th day, 7th day and 15th day

following parameters before and after the

时间窗: 0th day, 7th day and 15th day

treatment

时间窗: 0th day, 7th day and 15th day

Subjective parameters

时间窗: 0th day, 7th day and 15th day

Stiffness

时间窗: 0th day, 7th day and 15th day

Tingling sensation

时间窗: 0th day, 7th day and 15th day

Numbness

时间窗: 0th day, 7th day and 15th day

Pain by visual analogue scale

时间窗: 0th day, 7th day and 15th day

次要结局

  • Quality of life(0th day & 15th day)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Archana A S

Sri Dharamasthala Manjunatheshwara College Of Ayurveda Hospital and Research Centre Kuthpady Udupi

研究点 (1)

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