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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ISRCTN
Last refreshed on: 17 October 2016
Main ID:  ISRCTN29365316
Date of registration: 16/06/2015
Prospective Registration: No
Primary sponsor: Lagos University Teaching Hospital
Public title: Intrasound therapy and transcutaneous electrical nerve stimulation (TENS) in the treatment of osteoarthritis of the knee
Scientific title: Intrasound therapy is an effective adjunct in the management of osteoarthritis of the knee: a preliminary clinical study
Date of first enrolment: 29/07/2014
Target sample size: 32
Recruitment status: Completed
URL:  http://isrctn.com/ISRCTN29365316
Study type:  Interventional
Study design:  Single-centre preliminary clinical interventional study (Treatment)  
Phase: 
Countries of recruitment
Nigeria
Contacts
Name: Ayoola    Aiyegbusi
Address:  Department of Physiotherapy College of Medicine, University of Lagos 02341 Lagos Nigeria
Telephone:
Email:
Affiliation: 
Name:    
Address: 
Telephone:
Email:
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. Age 52-76
2. Unilateral OA of the knee

Exclusion criteria: 1. Patients with underlying systemic diseases and other rheumatic conditions of the knee
2. Patients with severe OA using the Kellgren and Lawrence system of classification


Age minimum:
Age maximum:
Gender: Both
Health Condition(s) or Problem(s) studied
Mild/moderate unilateral osteoarthritis of the knee
Musculoskeletal Diseases
Gonarthrosis
Intervention(s)
1. Group 1 (control): closed kinetic chain exercises and range of motion exercises
2. Group 2 (intervention): intrasound therapy for 10 minutes followed by closed kinetic chain exercises and range of motion exercises
3. Group 3 (intervention): TENS for 15 minutes followed by closed kinetic chain exercises and range of motion exercises
Primary Outcome(s)
Assessed pre-treatment, at baseline and post-treatment after 8 weeks of intervention: Western Ontario and McMaster Universities (WOMAC) score to assess pain, stiffness and physical function.
Secondary Outcome(s)
Assessed pre-treatment, at baseline and post-treatment after 8 weeks of intervention:
1. 6-minute walk test
2. Range of motion of the knee
Secondary ID(s)
N/A
Source(s) of Monetary Support
Investigator initiated and funded
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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