跳至主要内容
临床试验/CTRI/2025/05/086754
CTRI/2025/05/086754尚未招募2 期

Comparative evaluation of the effectsof Hijama bila Shart (Dry Cupping) &Hijama bish shart (Wet Cupping) incases of Waja-al-Unuq (Cervical Spondylosis)

Department of Ilaj Bit Tadbeer1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年5月26日最近更新:
适应症

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
•VAS (Visual Analogue Scale)[10]

研究概览

简要总结

Objective of the study:

1.)To evaluate the effects of Hijama bila Shart (Dry Cupping), in Waja-al Unuq

(Cervical Spondylosis).

2.)To evaluate the effects of Hijama bish shart (Wet Cupping), in Waja-al Unuq

(Cervical Spondylosis).

3.)To compare the effects of Hijama bila Shart (Dry Cupping) and Hijama bish

shart (Wet Cupping), in Waja-al Unuq (Cervical Spondylosis).

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

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

入选标准

  • •Clinically diagnosed patients of Waja’ al-Unuq (cervical spondylosis) 2)Patients who had given informed written consent and accepted to follow the protocol.
  • •Patients of both genders.
  • •Patients in the age group of 20-60 years.
  • •Cervical spondylosis with or without radiculopathy.

排除标准

  • •Patients below 20 years and above 60 years.
  • •Pregnant and lactating women.
  • •Patients of diabetes and hypertension.
  • •Patients with severe systemic illnesses.
  • •Patients unable to give informed written consent.
  • •Patient with nervous disorders like epilepsy & dizziness.
  • •Patient having concomitant therapy.
  • •Patient with thyroid disease.
  • •Patient requiring rescue medicine very frequently or once a week.

结局指标

主要结局

•VAS (Visual Analogue Scale)[10]

时间窗: 7th, 14th, 21st, 28th day

•Vernon and Mior Cervical Spine Questionnaire

时间窗: 7th, 14th, 21st, 28th day

•X- ray cervical spine Antero-posterior and Lateral view

时间窗: 7th, 14th, 21st, 28th day

次要结局

  • •Pain(•Tenderness)

研究者

发起方
Department of Ilaj Bit Tadbeer
申办方类型
Government medical college

研究点 (1)

Loading locations...

相似试验