Evaluation of the Effect of Pashoya Therapy on Pain Management and Functional Improvement in Plantar Fasciitis Patients
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- Numeric Pain Rating Scale (NPRS)
研究概览
简要总结
This research proposal aims to evaluate the therapeutic potential of Pashoya as a complementary treatment for plantar fasciitis. By conducting a clinical study to assess its impact on pain reduction, inflammation, and functional improvement, the study seeks to
determine whether Pashoya can provide effective relief and serve as a viable alternative or adjunct to conventional treatments. The findings could expand the current therapeutic options available to patients and contribute to a more integrative approach to managing plantar fasciitis.
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
- 18.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •Adults aged 18-65 years Clinically diagnosed with plantar fasciitis based on the presence of heel pain for at least three months.
- •Pain levels of at least 4 on a scale of 0 to 10 during initial assessment.
- •Willingness to participate in the study and provide informed consent.
排除标准
- •Aged less than 18 and more than 65 years History of surgical intervention for plantar fasciitis.
- •Recent treatment with corticosteroids or other anti-inflammatory medications within the last month.
- •Comorbid conditions affecting foot health (e.g., severe osteoarthritis, neuropathy).
- •Pregnancy or lactation.
- •Allergies to any components of Pashoya or placebo.
- •Patients with uncontrolled diabetes mellitus.
- •Patients with uncontrolled hypertension Assessment.
结局指标
主要结局
Numeric Pain Rating Scale (NPRS)
时间窗: Visit 1st : Baseline | Visit 2nd : 7th day | Visit 3rd : 14th day
Foot Function Index (FFI)
时间窗: Visit 1st : Baseline | Visit 2nd : 7th day | Visit 3rd : 14th day
次要结局
- Heel pain particularly in the morning or following inactivity during the day(Stiffness of foot)
研究者
SAIMA NUZHAT MOHAMMADI
AJMAL KHAN TIBBIYA COLLEGE & HOSPITAL