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临床试验/CTRI/2024/10/074673
CTRI/2024/10/074673尚未招募2 期

Clinical study to Evaluate Efficacy and Tolerability of Shwashkuthar Ras (Pradhman Nasya) in Vatika Shiroroga

Gurukul Campus UAU Haridwar1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年10月20日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Relief in Subjective Parameters like:

研究概览

简要总结

This study is a single-arm, open-label trial for the Efficacy and Tolerability of Shwashkuthar Ras Pradhman Nasya in Vatika Shiroroga. This study will be conducted at UAU Gurukul Campus Haridwar in 30 Patients. The assessment will be done based on Subjective Parameters. The study will be conducted at the OPD/IPD level of the PG Department of Panchakarma.

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 50.00 Year(s)(—)
性别
All

入选标准

  • •Patients from the Age group between 20-
  • •Patient will be selected irrespective of sex, religion, occupation etc.
  • •Patients with classical signs and symptoms of Vatika Shiroroga will be selected from OPD and IPD of Gurukul campus hospital UAU Haridwar.
  • •Patients fulfilling ICHD3 criteria for Tension-Type of Headache 5) Patients previously treated with medicines or therapies for Vatika Shirorog.

排除标准

  • •Known case of Sinusitis 2)Any other types of infections associated with fever.
  • •Any pathology involving the eyes.
  • •Uncontrolled Hypertension 5) Diabetes mellitus 6)Migraine, Cluster headache, Trigeminal neuralgia 7)Known cases of Seizures 8)Any other serious systemic illness.
  • •Secondary headache arising due to meningitis, tumor, cervical spondylosis, etc.
  • •Patients who are intolerant to Pradhman Nasya.

结局指标

主要结局

Relief in Subjective Parameters like:

时间窗: 1st day,35 day

1) Bitemporal Headache

时间窗: 1st day,35 day

2) Pain in the Occipital Region

时间窗: 1st day,35 day

3) Pain and burning in the Frontal region

时间窗: 1st day,35 day

4) Pain in eyes as if eyes are coming out

时间窗: 1st day,35 day

5) Severe Pain in the Ears

时间窗: 1st day,35 day

6) Giddiness

时间窗: 1st day,35 day

7) Pain as if joints are laxed

时间窗: 1st day,35 day

8) Disturbed sleep

时间窗: 1st day,35 day

9) Excessive pain at night

时间窗: 1st day,35 day

次要结局

  • Relief in sign and symptoms of Vatika Shiroroga(1st, 35th day)

研究者

发起方
Gurukul Campus UAU Haridwar
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Pratibha Nawani

Gurukul Campus UAU Haridwar

研究点 (1)

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