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临床试验/CTRI/2024/07/070613
CTRI/2024/07/070613尚未招募2 期

Clinical Efficacy of Dalk Mutadil (Moderate Massage) with Rogan-E-Qust in The Management of Irqun Nasa (Sciatica)

Government Unani Medical College Chennai1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2024年7月25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
33
试验地点
1
主要终点
Reduction in clinical symptoms, Change in subjective parameters, on Visual Analogue Scale (VAS)

研究概览

简要总结

Efficacy of Dalk Mu’tadil with Rogan-e-Qust in the management of Irqun-Nasa (Sciatica).

Duration: 28 days

Sample size: 30

IEC No:GUMC/IEC/2022-2023/MJ/23/05

Outcome:

Primary Outcome: The outcome will be mainly assessed by reduction in clinical symptoms after the treatment and assessing the improvement of the patient from severe to moderate, moderate to mild.

SECONDARY OUTCOME:

Radiological Parameters, if required

Objective of the study: To assess the role of clinical efficacy of “Dalk with Rogan Qust” in the management of Irqun-nasa.

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 60.00 Year(s)(—)
性别
All

入选标准

  • 1.Age from 20 to 60 years (Sine saba and Sine Kahulat ) 2.Patients of either sex between the ages of 20 to 60 years 3.Already diagnosed patients of sciatica presenting with all or some of the following signs and symptoms a.
  • Unilateral leg pain greater than low back pain b.
  • Pain radiating to foot or toes c.
  • Tingling, pins and shooting pain d.
  • Numbness or paraesthesia in the same distribution.

排除标准

  • 1.Patient below 20 years and above 60 years of age
  • Patient of spinal deformities
  • Patient of previous back surgery/lumbar spine surgery
  • Patient with bleeding disorders
  • Patient on anticoagulant treatment or DIC (Disseminated intravascular coagulopathies
  • Patients with systemic disorders like uncontrolled diabetes mellitus, chronic liver disease, kidney disease, heart disease (CAD, ACS)
  • Terminally ill patient
  • Pregnant and lactating mother.

结局指标

主要结局

Reduction in clinical symptoms, Change in subjective parameters, on Visual Analogue Scale (VAS)

时间窗: 28 Days

SLR Test

时间窗: 28 Days

次要结局

  • Improvement in Quality of life on objective parameters-(Oswestry disability index (ODI))

研究者

发起方
Government Unani Medical College Chennai
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Anwarul Haq

Government Unani Medical College, Chennai

研究点 (1)

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