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NCT05925855 Clinical Trial

Effect of Phonophoresis on Trigger Points

Trigger Point Pain, Myofascial Clinical Trial

Official title:
Effect of Phonophoresis on Trigger Points

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT05925855
Other study ID # Phonophoresis
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 2023
Est. completion date September 2023

Study information
Verified date July 2023
Source Batterjee Medical College
Contact Reem S Dawood, PhD
Phone +966126562415
Email pt9.jed@bmc.edu.sa
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Description:

participants will be divided into 3 groups, 2 study groups and 1 control group.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 20
Est. completion date September 2023
Est. primary completion date August 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - upper trapezius trigger point Exclusion Criteria: - cervical disc

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• US with fastum
apply fastum on trigger point with US
• US with reparil
apply reparil on trigger point with US
• US with plain gel
apply gel on trigger point with US

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Batterjee Medical College

Outcome
Type Measure Description Time frame Safety issue
Primary pain intensity change of pain intensity by using VAS from 0 to 10 Two weeks
Primary pain threshold change of pain threshold by using PPA two weeks
Primary ROM change of ROM by using CROM two weeks
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