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NCT02649296 Clinical Trial

Effect of Skanlab Regarding Knee Arthrosis

Arthrosis Clinical Trial

Official title:
Effect of Skanlab Regarding Knee Arthrosis

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02649296
Other study ID # Skanlab
Secondary ID
Status Recruiting
Phase N/A
First received October 29, 2015
Last updated September 27, 2016
Start date October 2015
Est. completion date December 2016

Study information
Verified date September 2016
Source Oslo and Akershus University College of Applied Sciences
Contact Hilde Sylliaas, Ass prof
Email hilde.sylliaas@hioa.no
Is FDA regulated No
Health authority Norway: Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose is to find out the effect of Skanlab at knee arthrosis.

Description:

The patients diagnosed with knee arthrosis will be treated With Skanlab twice a week for four weeks.

Recruitment information / eligibility
Status Recruiting
Enrollment 16
Est. completion date December 2016
Est. primary completion date January 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 45 Years to 70 Years
Eligibility Inclusion Criteria:

- knee arthrosis in one or both legs

Exclusion Criteria:

- Pacemaker

- infusion pump

- cancer

- diabetes

- pregnancy

- blood clots

- bacteriological inflammation

- reduced sensitivity in the treatment area.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor)

Related Conditions & MeSH terms

Intervention

Other:
• Skanlab bodywave
The intervention will be done twice a week

Locations
Country Name City State
Norway Oslo and Akershus University college of applied science Oslo

Sponsors (1)
Lead Sponsor Collaborator
Oslo and Akershus University College of Applied Sciences

Country where clinical trial is conducted

Norway, 

Outcome
Type Measure Description Time frame Safety issue
Primary Knee injury and Osteoarthritis Outcome Score (KOOS) changes in pain 15 months No
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