College of Medicine
Ismailia, 41522, Egypt
NCT Number: NCT06573775
To evaluate pain quality by pain quality assessment scale (PQAS) using lidocaine phonophoresis on myofascial pain syndrome (MPS) in athletic children.
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Notify Me10 year–14 year
All sexes
Interventional
Not applicable
Ismailia, 41522, Egypt
Forty five males athletic swimmer children (10 to 14 years old) with MPS in the upper trapezius muscle were evaluated before and after treatment. They were randomly divided into three groups, n=15 children each. A (control), B and C (study groups). The three groups received spatial designed physical therapy program. The two study groups received pulsed ultrasound and lidocaine phonophoresis repectively. The duration of treatment was 40 minutes, three times / weeks for three successive months.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
treatment of myofacial trigger points with therapeutic ultrasound
manual massage and range of motion exercises
Other names: myofascial trigger point realease
transdermal tranmission of lidocaine molecules via ultrasound
Time frame: 6 weeks
pain quality assessment scale with zero indication of better outcome and twenty means the worst outcome
Time frame: 6 weeks
measurement of serum cortisol level
New Ismailia National University
Other
Evaluation of Pain Quality in Young Swimmers Suffering From Myofascial Pain Syndrome Using Lidocaine Phonophoresis: A Randomized Controlled Trial
Acronym: MPS
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