A study to compare the effect of Bloodletting with and without Oral Medication in the management of Plantar fasciitis
Phase 2
- Conditions
- Health Condition 1: M722- Plantar fascial fibromatosis
- Registration Number
- CTRI/2023/04/051846
- Lead Sponsor
- Dayanand Ayurvedic College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Subjects suffering from classical signs and symptoms of Vatakantaka as per Ayurvedic classical texts.
2. Diagnosed subjects of Plantar fasciitis according to clinical features.
3. Subjects between 16 to 70 years of age.
4. Male and female subjects willing and able to participate in the study.
Exclusion Criteria
1. Pregnant women and lactating women will be excluded.
2. Subjects having other major complicated systemic disorders.
3. Subjects with deranged BT and CT.
4. Subjects in whom Siravedha is contraindicated.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Reduced Visual Analog Scale (VAS) Score. <br/ ><br>2. Reduced tenderness. <br/ ><br>3. Negative Windlass test.Timepoint: Day 35: At the time of follow up
- Secondary Outcome Measures
Name Time Method 1. Reduced Visual Analog Scale (VAS) Score. <br/ ><br>2. Reduced tenderness. <br/ ><br>3. Negative Windlass test.Timepoint: Day 21: At the end of the treatment.