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Clinical Trials/NCT00155324
NCT00155324
Completed
Not Applicable

Change and Clinical Significance of Plantar Fascia Thickness After Extracorporeal Shock Wave Therapy

National Taiwan University Hospital1 site in 1 country60 target enrollmentOctober 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Plantar Fasciitis
Sponsor
National Taiwan University Hospital
Enrollment
60
Locations
1
Primary Endpoint
Thickness of plantar fascia by ultrasonographic examination at 3 & 6 months
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The aim of the study is to investigate the effect of extracorporeal shock wave therapy (ESWT) on the thickness of plantar fascia measured by ultrasonographic examination among patients with chronic plantar fascitis. The change of plantar fascia thickness will be correlated with clinical improvement.

Detailed Description

The aim of the study is to investigate the effect of extracorporeal shock wave therapy (ESWT) on the thickness of plantar fascia measured by ultrasonographic examination among patients with chronic plantar fascitis. Two different dosage of ESWT will be applied, and the outcome will be followed 3 and 6 months after the treatment. The change of plantar fascia thickness will be correlated with clinical improvement, including the pain improvement, foot function, and quality of life at follow up.

Registry
clinicaltrials.gov
Start Date
October 2004
End Date
July 2006
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • diagnosed as plantar fasciitis for at least 6 months
  • refractory to other conservative treatments

Exclusion Criteria

  • Acute infection of soft tissue/bone
  • Malignancy
  • Epiphysiolysis in the focus
  • Blood coagulation disorders
  • Pregnancy
  • Patients with pacemaker
  • Foot deformity
  • Autoimmune disorders-related arthropahy
  • Previous treatment with ESWT

Outcomes

Primary Outcomes

Thickness of plantar fascia by ultrasonographic examination at 3 & 6 months

Secondary Outcomes

  • Pain (visual analogue scale) at 3 & 6 months
  • Foot function index at 3 & 6 months
  • Short Form-36 at 3 & 6 months

Study Sites (1)

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