Effect of Phonophoresis on Trigger Points
Sponsor
Batterjee Medical College (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05925855
Collaborator
(none)
20
3
3
Study Details
Study Description
Brief 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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
participants will be divided into 3 groups, 2 study groups and 1 control group.
Study Design
Study Type:
Interventional
Anticipated Enrollment
:
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Effect of Phonophoresis on Trigger Points
Anticipated Study Start Date
:
Jun 1, 2023
Anticipated Primary Completion Date
:
Aug 1, 2023
Anticipated Study Completion Date
:
Sep 1, 2023
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: study Fastum participant in this group will receive US with fastum gel |
Other: US with fastum
apply fastum on trigger point with US
|
| Experimental: study Reparil participant in this group will receive US with reparil gel |
Other: US with reparil
apply reparil on trigger point with US
|
| Active Comparator: Control plain gel participant in this group will receive US with gel |
Other: US with plain gel
apply gel on trigger point with US
|
Outcome Measures
Primary Outcome Measures
- pain intensity [Two weeks]
change of pain intensity by using VAS from 0 to 10
- pain threshold [two weeks]
change of pain threshold by using PPA
- ROM [two weeks]
change of ROM by using CROM
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 35 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- upper trapezius trigger point
Exclusion Criteria:
- cervical disc
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Batterjee Medical College
Investigators
- Study Director: Osama R Abdelraouf, PhD, Batterjee Medical College
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Reem Dawood,
Assistant professor,
Batterjee Medical College
ClinicalTrials.gov Identifier:
NCT05925855
Other Study ID Numbers:
- Phonophoresis
First Posted:
Jun 29, 2023
Last Update Posted:
Jul 3, 2023
Last Verified:
Jun 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms: