Bone Marrow Aspirate Versus Platelet-Rich Fibrin for the Treatment of Chronic Plantar Fasciitis
72 patients around the world
Available in Brazil
Chronic plantar fasciitis is a common cause of heel pain that may persist despite
standard conservative measures such as physical therapy, stretching, orthoses, and
corticosteroid injections. Regenerative medicine techniques, including autologous
platelet concentrates and bone marrow-derived products, have emerged as potential
alternatives to promote tissue healing and long-term symptom improvement.
This randomized controlled trial investigates and compares two minimally invasive
orthobiologic interventions:
Bone Marrow Aspirate (BMA) - obtained from the posterior iliac crest under local
anesthesia and injected into the most symptomatic region of the plantar fascia under
ultrasound guidance.
Platelet-Rich Fibrin (PRF) - prepared from autologous venous blood by centrifugation
without anticoagulants, forming a fibrin matrix injected into the plantar fascia under
ultrasound guidance.
All procedures are performed under sterile conditions and tibial nerve regional
anesthesia.
Pain and safety will be monitored using the Visual Analog Scale (VAS) and by recording
adverse events at the following time points: baseline (0), 30 minutes, 1, 6, 12, and 24
months after the procedure.
Functional outcomes will be collected with Modified AOFAS Score at baseline, 1, 6, 12,
and 24 months. Ultrasonography will measure plantar fascia thickness immediately before
the intervention and at 12 months.
This research contributes to the growing evidence supporting orthobiologic therapies as
viable, minimally invasive options for chronic plantar fasciitis management.
Federal University of São Paulo
1Research sites
72Patients around the world
This study is for people with
Fasciitis
Plantar fasciitis
Requirements for the patient
To 75 Years
All Gender
Medical requirements
Adults aged 18 to 75 years.
Clinical diagnosis of chronic plantar fasciitis for more than 6 months, confirmed by ultrasonography (increased plantar fascia thickness and hypoechogenicity).
Persistent heel pain refractory to conventional conservative treatment (stretching, orthotics, physical therapy, or corticosteroid injections).
Visual Analog Scale (VAS) pain score ≥ 4 at baseline.
Ability and willingness to comply with study procedures and follow-up assessments.
Signed informed consent.
Previous foot or ankle surgery on the affected limb.
Acute trauma, infection, or ulceration in the region of the plantar fascia.