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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00155324
Other study ID # 9361701153
Secondary ID
Status Completed
Phase N/A
First received September 8, 2005
Last updated November 30, 2012
Start date October 2004
Est. completion date July 2006

Study information

Verified date November 2012
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 19 Years and older
Eligibility 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

- Sciatica

- Previous treatment with ESWT

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Extracorporeal Shock Wave Therapy (Device)


Locations

Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Thickness of plantar fascia by ultrasonographic examination at 3 & 6 months
Secondary Pain (visual analogue scale) at 3 & 6 months
Secondary Foot function index at 3 & 6 months
Secondary Short Form-36 at 3 & 6 months
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