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The effect of autologous blood on plantar fasciitis

Phase 3
Recruiting
Conditions
plantar fasciitis.
Plantar fascial fibromatosis
M72.2
Registration Number
IRCT20160508027797N7
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
90
Inclusion Criteria

Age over 18 years
Heel pain for at least 4 weeks
Pain intensity greater than 5 based on visual analog scale index
Tenderness at the junction of plantar fascia with calcaneus
Having the ability to follow up for 6 months after starting treatment
Conscious written consent

Exclusion Criteria

Heel surgery
Evidence in favor of calcaneus fracture
Nerve damage
Achilles tendon injury
Rheumatoid Arthritis
Local or systemic infection
Peripheral vascular disorder
Gout
Coagulation disorder
Pregnancy or breastfeeding
Corticosteroid injection in the last 3 months
Use of non-steroidal anti-inflammatory drugs in the last 7 days
History of allergy to injectable solutions

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain control by autologous blood injection. Timepoint: First week, fourth week, third month, sixth month. Method of measurement: visual analogue scale index, role and maudsley scale.
Secondary Outcome Measures
NameTimeMethod
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