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Clinical Trials/DRKS00009392
DRKS00009392
Completed
N/A

The effect of a novel orthotic device on the physical activity levels in the daily life of patients with medial knee osteoarthritis - KNEEMO

Funktionsbereich BewegungsanalytikKlinik und Poliklinik für Allgemeine Orthopädie und TumororthopädieUniversitätsklinikum Münster0 sites52 target enrollmentDecember 3, 2015
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ConditionsM17Gonarthrosis [arthrosis of knee]

Overview

Phase
N/A
Intervention
Not specified
Conditions
M17
Sponsor
Funktionsbereich BewegungsanalytikKlinik und Poliklinik für Allgemeine Orthopädie und TumororthopädieUniversitätsklinikum Münster
Enrollment
52
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 3, 2015
End Date
July 1, 2017
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
Funktionsbereich BewegungsanalytikKlinik und Poliklinik für Allgemeine Orthopädie und TumororthopädieUniversitätsklinikum Münster

Eligibility Criteria

Inclusion Criteria

  • •Eligible adults will be required to have clinical KOA according to the American College of Rheumatology guidelines, with knee pain \= 4 days per week for \=3 months

Exclusion Criteria

  • •Exclusion criteria will be:
  • •\- Rheumatoid arthritis or any other form of inflammatory arthritis (e.g. crystal arthropathy)
  • •\- Diabetes
  • •\- Knee replacement, or a scheduled replacement surgery within 3 months in affected leg from or before the beginning of study participation.
  • •\- Medical conditions, which could interfere with the activity and test performance, such as neurologic conditions or severe cardiovascular disease.
  • •\- Use of ambulatory aid (single straight cane)

Outcomes

Primary Outcomes

Not specified

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