Achilles tendon injury: investigation of stabilisation footwear used for medical treatment
Not Applicable
- Conditions
- S86.0Injury of Achilles tendon
- Registration Number
- DRKS00015434
- Lead Sponsor
- Zürcher Hochschule für Angewandte Wissenschaften
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting stopped after recruiting started
- Sex
- All
- Target Recruitment
- 14
Inclusion Criteria
Informed Consent as documented by signature
- Age: 18 – 60 years
- Body mass index: 18 – 28 kg/m2
Patient group only:
- Currently wearing VACOped, Orthotech Vario-Stabil, or Künzli Ortho Rehab Absolut following Achilles tendon injury
- Walk without crutches, full-weight bearing allowed
Exclusion Criteria
- Women who are pregnant or breast feeding
- Previous enrolment into the current study
- Enrolment of employees and other dependent persons associated with the investigational
product or control product
- Acute or chronic musculoskeletal diseases (except Achilles tendon injury for patient group)
- Acute or chronic cardiovascular diseases
- Acute or chronic neurological disease
Control group only
- Previous Achilles tendon injury
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method