A study to compare the effect of blood component and dextrose injection in patients of chronic severe plantar fasciitis

Phase 2

• Conditions: Health Condition 1: null- Plantar fasciitis

• Registration Number: CTRI/2018/02/012220
• Lead Sponsor: Krishna B

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Patient diagnosed with unilateral or bilateral plantar fasciitis having no improvement with conservative management for >= 3 weeks.

2.Physical examination revealing maximum tenderness at the attachment of plantar fascia on the medial tubercle of the calcaneus.

3.Ultrasound examination showing plantar fascia thickness >=4 mm or difference in plantar fascia thickness >=1 mm in symptomatic heel in comparison to asymptomatic heel at inferior border of the calcaneus.

4.In bilateral cases, foot with more clinical severity is taken into the study

Exclusion Criteria

1.Received local steroid injection within 6 months

2. NSAID use 7 days prior to randomization

3. History of anaemia or bleeding disorders

4. Previous surgery for plantar fasciitis

5. Achilles tendon pathology

6.Diagnosed case of local malignancy

7.Diagnosed case of rheumatological diseases

8.Uncontrolled diabetes mellitus

9.Patients on anticoagulation therapy

10. Diagnosis of vascular insufficiency or neuropathy related heel pain (radiculopathy, tarsal tunnel syndrome) and other causes of heel pain

11. Any local trauma or infection.

12.Not willing to participate in study

Study & Design

• Study Type: Interventional
• Study Design: Not specified