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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05224674
Other study ID # Van Yuzuncu Yil University
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2022
Est. completion date September 30, 2022

Study information

Verified date November 2022
Source Yuzuncu Yil University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is no scientific study in the literature regarding the use of shock wave therapy in hip osteoarthritis. In this study, we aim to investigate both the effectiveness of ESWT and which type of ESWT can be more effective in hip osteoarthritis.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date September 30, 2022
Est. primary completion date August 29, 2022
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - unilateral or bilateral hip osteoarthritis Exclusion Criteria: - other disorders that are contraindications for shockwave therapy, not have received ESWT treatment before

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Extracorporeal Shock Wave Therapy (ESWT)
The ESWT device is product of Elettronica Pagani, Italy.

Locations

Country Name City State
Turkey Volkan Sah Van

Sponsors (1)

Lead Sponsor Collaborator
Yuzuncu Yil University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale (VAS) patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse outcome. at baseline.
Primary Visual Analogue Scale (VAS) patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse outcome 4 weeks after baseline.
Primary Visual Analogue Scale (VAS) patient's self-assessment of pain, in the range of 0 to 10, higher scores mean a worse outcome. 8 weeks after baseline.
Secondary Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) 24-item questionnaire for osteoarthritis, in the range of 0 to 96, higher scores mean a worse outcome at baseline.
Secondary Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) 24-item questionnaire for osteoarthritis, in the range of 0 to 96, higher scores mean a worse outcome 4 weeks after baseline.
Secondary Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) 24-item questionnaire for osteoarthritis, in the range of 0 to 96, higher scores mean a worse outcome 8 weeks after baseline.
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