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Clinical Trials/ACTRN12617000675325
ACTRN12617000675325
Terminated
N/A

The correlation of changes in the neural mechanisms associated with pain and patient reported improvement in pain and function in mid-portion Achilles tendinopathy: A mechanistic cohort study

The University of Notre Dame Australia0 sites9 target enrollmentMay 10, 2017
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ConditionsMid-Portion Achilles TendinopathyMusculoskeletal - Other muscular and skeletal disordersPhysical Medicine / Rehabilitation - Physiotherapy

Overview

Phase
N/A
Intervention
Not specified
Conditions
Mid-Portion Achilles Tendinopathy
Sponsor
The University of Notre Dame Australia
Enrollment
9
Status
Terminated
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 10, 2017
End Date
March 31, 2020
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Recreational or competitive runner
  • •\*Can have ceased running due to AT
  • •\*No limit on distance or running duration per week
  • •Reported pain for greater than 3 months
  • •Reported local Achilles Pain (\<2 fingers width)
  • •Reported local Achilles Stiffness
  • •Reported impairment of functional activity
  • •\*Local A\-P Thickening of the mid\-portion AT
  • •\*Hyperechoic area of the mid\-tendon with colour Doppler signal within the area
  • •Ability to given informed consent

Exclusion Criteria

  • •\- VISA\-A score of greater than 80/100, 12 week wash out from other treatments,
  • •\- Corticosteroid injection within the past 12 months,
  • •\- Bilateral Achilles Tendinopathy,
  • •\- Insertional Achilles Tendinopathy,
  • •\- Previous Fracture lower limb within 12 months,
  • •\- Systemic Disease (Diabetes, Rheumatic Conditions, Circulatory Disorders, Neurological Disorders),
  • •\- Foot or Ankle Surgery in the previous 6 months,
  • •\- Regular intake of medication which may have an influence on outcome (Statins, Fluoroquinolones),
  • •\- Confounding lower limb or ankle injury,
  • •\- Confounding Injury for CPM (chronic lumbar pain, recurrent or chronic tension headache, migraine, whiplash, painful OA etc),

Outcomes

Primary Outcomes

Not specified

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