M16
Conditions
Interventions
Group 1: Standard postoperative physiotherapy plus three additional 20-minute sessions of standardized myofascial osteopathic treatment during the first postoperative week.
Group 2: Standard postopera
Sponsors
Universitätsklinikum Düsseldorf Klinik für Orthopädie und Unfallchirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in postoperative pain intensity measured by the Visual Analogue Scale (VAS, 0–10) during the inpatient period. | — |
Secondary
| Measure | Time frame |
|---|---|
| Harris Hip Score (HHS) High-Activity Arthroplasty Score (HAAS) Hip Disability and Osteoarthritis Outcome Score (HOOS) Analgesic consumption according to WHO analgesic ladder (steps I–III) Patient-reported outcomes at six-week follow-up | — |
Countries
Germany
Contacts
Public ContactMarcel Höpfner
Universitätsklinikum Düsseldorf Klinik für Orthopädie und Unfallchirurgie
Outcome results
None listed