Efficacy of dextrose prolotherapy in the treatment of plantar fasciitis
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- 3. Plantar fascia thickness
研究概览
简要总结
This study is an interventional cohort study to study the efficacy of dextrose prolotherapy in plantar fasciitis patients in relation to pain, foot function index and plantar fascia thickness. The study will be conducted in out-patient department of Physical Medicine and Rehabilitation, VMMC & Safdarjung Hospital, New Delhi. Clinically diagnosed cases of plantar fasciitis will be enrolled in the study after applying inclusion criteria and taking informed consent. Baseline investigations will be done before intervention. Patients will undergo USG guided prolotherapy under all aseptic conditions. Patients will be clinically evaluated using numeric pain rating scale, foot function index and plantar fascia thickness on baseline day 0, week 2 and week 8. After getting clinical evaluation scores pre and post intervention data will be compiled in a tabular form.
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 18.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Clinically diagnosed cases of plantar fasciitis with duration of symptoms more than 3 months.
排除标准
- •Recent history of trauma and calcaneal fracture
- •Prior injection treatment for heel pain within 6 months
- •Prior surgery for plantar fasciitis
- •Active infection at injection site
- •Uncontrolled diabetes mellitus
- •Bleeding disorders
- •Dementia and other psychiatric illness.
结局指标
主要结局
3. Plantar fascia thickness
时间窗: At 0, 2 and 8 weeks
1. Pain using Numeric Pain Rating Scale
时间窗: At 0, 2 and 8 weeks
2. Foot function using Foot Function Index
时间窗: At 0, 2 and 8 weeks
次要结局
- Plantar fascia thickness on USG(At 0, 4 and 8 week)