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NCT01429883 Clinical Trial

Extracorporeal Shock Wave Treatment - Can the Pain be Reduced?

Fasciitis, Plantar Clinical Trial

Official title:
Extracorporeal Shock Wave Treatment - Can the Pain be Reduced?

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01429883
Other study ID # ESWTRUZ01
Secondary ID
Status Completed
Phase Phase 4
First received September 5, 2011
Last updated June 2, 2015
Start date July 2011
Est. completion date January 2015

Study information
Verified date May 2015
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

Patients with Fascititis plantaris, Achillodynie, Periarthropathia humerosacpularis calcarea or Epikondylopathia humeri /radii get the shock wave therapy in our clinic as planned. During our study the investigators want to ask for pain, pain reduction and function.

Description:

Patients with either Fascititis plantaris, Achillodynie, Periarthropathia humerosacpularis calcarea or Epikondylopathia humeri /radii get a shock wave therapy in our clinic of rheumatology as planned. During our study the investigators ask for pain, pain reduction and function (all questionnaires).

Recruitment information / eligibility
Status Completed
Enrollment 36
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

-Patients with:

- Fascititis plantaris,

- Achillodynie,

- Periarthropathia humerosacpularis calcarea or

- Epicondylopathia humeri /radii, who got the shock wave therapy.

Exclusion criteria:

- Anticoagulation,

- Sepsis

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Switzerland University Hospital Zurich

Sponsors (1)
Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

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