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The influence of myofascial techniques in addition to standard-physiotherapy on patients with cox-, gon- and omarthrosis after endoprosthesis-implantation : a comparative prospective clinical trial

Conditions
M16
M17
M19
Coxarthrosis [arthrosis of hip]
Gonarthrosis [arthrosis of knee]
Other arthrosis
Registration Number
DRKS00020366
Lead Sponsor
niversitätsklinikum Düsseldorf Klinik für Orthopädie und Unfallchirurgie
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
67
Inclusion Criteria

the patient is at least 18 years old
- written consent by the patient
- primary or secondary cox-, gon- or omarthrosis
- planned implantation of an endoprosthesis (hip, shoulder or knee)
- approval for surgery by the orthopedist and anesthetist

Exclusion Criteria

- oncological disease
- immunosupression
- rheumatic disease
- infections (systemic or in the treated area)
- chronic pain
- dysfunctions of the joints caused by neurological disease
- pregnancy or lactation period
- patient can't undergo the surgery

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain measured with the Visual analogue scale before and after every of the four treatments (altogether eight times).
Secondary Outcome Measures
NameTimeMethod
- activities of daily living are measured with a questionnaire before endoprosthesis implantation and after six weeks as part of the follow-up (Hip: Included in the Harris Hip Score)<br>- range of motion with neutral zero method before and after every of the four interventions (altogether eight times)<br>- tension in muscles (relaxed or contracted), tendons, ligaments and fascial tissue with MyotonPro and TensioMyoGraph before and after every of the four interventions (altogether eight times)<br>
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