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NCT03857334 Clinical Trial

Efficacy of Platelet Rich Plasma in Plantar Fasciitis

Plantar Fascitis Clinical Trial

— APOPLANT  

Official title:
Plantar Fasciitis Treatment: Double Blinded Randomized Control Study of the Efficacy of an Injection of Platelet Rich Plasma (PRP) Versus an Infiltration of Corticosteroids

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03857334
Other study ID # UF 8737
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 1, 2016
Est. completion date December 31, 2018

Study information
Verified date February 2019
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Plantar fasciitis is a common pathology among podiatry moreover the healing time takes several months.

The main aim of this study is to evaluate the efficacy of a injection of Platelet-Rich Plasma (PRP) versus corticosteroid injection.

Recruitment information / eligibility
Status Completed
Enrollment 50
Est. completion date December 31, 2018
Est. primary completion date October 18, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Plantar fasciitis

- Average VAS greater than or equal to 5/10

- Resistance of medical reference treatment

Exclusion Criteria:

- Other plantar lesion find on RMI

- Pregnancy

Study Design

Related Conditions & MeSH terms

Intervention

Biological:
• Injection of autologous platelet rich plasma

Drug:
• Injection of cortivazol : Altim®
Corticosteroids

Locations
Country Name City State
France Montpellier University Hosîtal Montpellier

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mean daily pain measured with a visual analog scale from 0 to 10 Comparison of pain intensity, measured with a visual analog scale from 0 to 10 6 months
Secondary Pain intensity during the first steps of the day measured with a visual analog scale from 0 to 10 Measured with a visual analog scale from 0 to 10 6 months
Secondary Pain intensity on direct compression measured with a visual analog scale from 0 to 10 Constant intensity of the compression, measured with a visual analog scale from 0 to 10 6 months
Secondary Impairment of walking function Foot function index 6 months
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