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Platelet Rich Plasma
RCT Comparing ESWT With PRP for Plantar Fasciitis in High Demand Cohort
N/A
Waitlist Available
Led By Amanda L Allen, MD
Research Sponsored by William Beaumont Army Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3, 6, 12, 24 weeks
Summary
A Randomized Controlled Pilot Trial Comparing Extracorporeal Shock Wave Therapy with Platelet Rich Plasma versus Extracorporeal Shock Wave Therapy in a High Demand Cohort with Resistant Plantar Fasciitis
Eligible Conditions
- Plantar Fasciitis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3, 6, 12, 24 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3, 6, 12, 24 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Visual analog scale (VAS)
Secondary study objectives
Functional Ankle Ability Measure (FAAM)
Functional Ankle Ability Measure extended sports scale
repeat treatment threshold
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Platelet Rich Plasma Injection GroupExperimental Treatment1 Intervention
shockwave therapy within standard of care using Ossatron system with intervention injection of platelet rich plasma (PRP) using Arthex system, into the plantar fascia at the calcaneal origin
Group II: Placebo injection groupPlacebo Group1 Intervention
shockwave therapy with placebo normal saline injection
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
platelet rich plasma
2014
Completed Phase 4
~760
Find a Location
Who is running the clinical trial?
William Beaumont Army Medical CenterLead Sponsor
16 Previous Clinical Trials
2,316 Total Patients Enrolled
Amanda L Allen, MDPrincipal InvestigatorWBAMC
Lola NortonStudy DirectorWBAMC
Timothy B Pekari, DScPrincipal InvestigatorWBAMC