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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05484752
Other study ID # ApiphanRama
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 1, 2019
Est. completion date March 30, 2020

Study information

Verified date August 2022
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To investigate effects of repetitive peripheral magnetic stimulation (PMS) on pain reduction in knee osteoarthritis


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date March 30, 2020
Est. primary completion date August 1, 2019
Accepts healthy volunteers No
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - Primary knee osteoarthritis patients who have had knee pain for at least 6 months and age more than 50 years, had morning stiffness not more than 30 minutes or crepitation. - Kellgren and Lawrence classification 2-4 - Visual analog scale of pain 4 or higher. Exclusion Criteria: - Patients with other musculoskeletal problems associated with knee joint - Patient with history of physical therapy in past 1 month - Patient with pacemaker, cochlear implant or cerebral shunt - Patient with history of knee surgery - Patient with neurological or other severe disease - Patient with previous seizure.

Study Design


Intervention

Device:
Repetitive Peripheral Magnetic Stimulation
Repetitive Peripheral Magnetic Stimulation at knee joint 1 session
Behavioral:
Education
Conventional exercise and life style modification

Locations

Country Name City State
Thailand Physical medicine and rehabilitation Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

References & Publications (1)

Pujol J, Pascual-Leone A, Dolz C, Delgado E, Dolz JL, Aldomà J. The effect of repetitive magnetic stimulation on localized musculoskeletal pain. Neuroreport. 1998 Jun 1;9(8):1745-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Visual analog scale Pain measurement Score from 0-10, 0 means no pain and 10 means maximum pain. Higher scores mean worse outcome. Change from baseline Visual analog scale at immediately after intervention and Change from Baseline visual analog scale at 1 week.
Secondary Modified Western Ontario and McMaster University Osteoarthritis Index To assessing pain, stiffness, and function in patients with osteoarthritis. Score from 0-220. Higher scores mean worse outcome. Change from Baseline Modified Western Ontario and McMaster University Osteoarthritis Index at 1 week.
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