Batterjee Medical College
Jeddah, Saudi Arabia
NCT Number: NCT05925855
purpose of this study was to investigate the effects of phonophoresis with fastum gel versus reparil gel on pain intensity, pain threshold, and cervical ROM of participant with trigger point of upper trapezius.
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Notify Me18 year–35 year
All sexes
Interventional
Not applicable
Jeddah, Saudi Arabia
participants will be divided into 3 groups, 2 study groups and 1 control group.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
apply fastum on trigger point with US
apply reparil on trigger point with US
apply gel on trigger point with US
Time frame: Two weeks and 3 months follow up
change of pain intensity by using VAS from 0 to 10
Time frame: two weeks and 3 months follow up
change of pain threshold by using PPA
Time frame: two weeks and 3 months follow up
change of ROM by using CROM
Time frame: Two weeks and 3 months follow up
change of neck function by using Neck Disability Index (NDI) questionnaire
Batterjee Medical College
Other
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