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Clinical Trials/NCT04376294
NCT04376294
Completed
Not Applicable

Using of Extracorporeal Shockwave Therapy in Treatment Of Achilles Tendinopathy

Cairo University1 site in 1 country50 target enrollmentOctober 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Achilles Tendinopathy
Sponsor
Cairo University
Enrollment
50
Locations
1
Primary Endpoint
The Victorian Institute of Sport Assessment-Achilles questionnaire (VISA-A).
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study was to determine the effect of extracorporeal Shock wave therapy (ESWT) on functional activity and pain in patients with Achilles tendinopathy

Detailed Description

Fifty patients of both sexes with Achilles tendinopathy aged 18-40 years, were assigned randomly into two equal groups. The study group received ESWT in addition to a conservative physical therapy program for four weeks, while the control group received a conservative physical therapy program only. Pain and functional mobility were assessed before and after treatment through a visual analog scale (VAS) and Victorian Institute of sports assessment - Achilles questionnaire (VISA-A), respectively

Registry
clinicaltrials.gov
Start Date
October 1, 2018
End Date
June 1, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Nasr Awad Abdelkader Othman

Lecturer

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Patients underwent physical therapy in the four weeks prior enrollment to study.
  • Patients had taken non-steroidal anti-inflammatory medication during the previous week
  • Patients had received peritendinous injections of a local anesthetic or corticosteroid within last 4 weeks
  • Patients had bilateral Achilles tendinopathy
  • Patients with other conditions that could significantly contribute to posterior ankle pain (osteoarthritis, radiculopathy, systemic neurologic conditions)
  • Patients having previous injury or surgical treatments of the ankle.

Outcomes

Primary Outcomes

The Victorian Institute of Sport Assessment-Achilles questionnaire (VISA-A).

Time Frame: 15 minutes

It consists of eight questions that covered the three domains of pain (questions 1-3), function (questions 4-6), and activity (questions 7 and 8.). Questions one to seven are scored out of 10, and question 8 carries a maximum of 30. Scores are summed to give a total out of 100.

Secondary Outcomes

  • The visual analog scale (VAS).(15 minutes)

Study Sites (1)

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