Chronic Plantar Fasciitis Clinical Trial
Official title:
Sonoelastographic Changes After Low Energy Extracorporeal Shock Wave Therapy (ESWT) in Plantar Fasciitis
Extracoporeal shock wave therapy(ESWT) was perfomed on the plantar fascia of chornic plantar fasciitis patients. Pre-ESWT and post-ESWT pain intensity, sonography and sonoelastrography of the plantar fascia was checked. Our hypothesis is that the plantar fascia stiffness increased after ESWT as clinical symptom improves.
For patient who met the inclusion criteria, we check sonography and sonoelastography for
their plantar fascias and obtain a thorough evulation questionaire for clinical symptom and
pain condition and intensity in various conditions, also SF-36 questionaire first. Inform
consent was done.
After the ESWT, we follow patient with questionaire and sonography/sonoelastography at
1-week, 1-month, 3-month, 6-month, 9-month, and 12-month post-ESWT time.
The colored sonoelastographic image was analysed by computer software "Image-J" with hue
analysis method and relative stiffness of selected area within proximal plantar fascia wasa
obtained for statistical analysis.
;
Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT01614223 -
Autologous Conditioned Plasma (ACP) for Patients With Plantar Fasciitis
|
N/A | |
Completed |
NCT03255655 -
Intense Therapeutic Ultrasound - Treatment for Chronic Plantar Fascia Musculoskeletal Pain Reduction
|
N/A | |
Completed |
NCT06348017 -
Frequency of Neuropathic Pain in Patients With Plantar Fasciitis
|
||
Recruiting |
NCT05868577 -
Infracalcaneal Peppering Injection Technique for Chronic Plantar Fasciitis
|
Phase 1 | |
Recruiting |
NCT03938896 -
PRP IN Planter Fascitis
|
N/A | |
Recruiting |
NCT05032300 -
Shear Wave Elastography Technology to Evaluate the Efficacy of ESW in the Treatment of Patients With Chronic Plantar Fasciitis
|
N/A | |
Completed |
NCT05754697 -
IASTM Versus PRT in Patients With Chronic PF
|
N/A | |
Completed |
NCT00447876 -
Study to Assess the Efficacy and Safety of Dysport® in the Treatment of Chronic Plantar Fasciitis
|
Phase 2/Phase 3 | |
Active, not recruiting |
NCT05162144 -
Proximal Medial Gastriocnemius Recession for Chronic Plantar Fasciitis
|
N/A |