Comparative Efficacy of Magnesium Sulfate Iontophoresis and Extracorporeal Shockwave Therapy on Chronic Mechanical Neck Pain
1 other identifier
interventional
100
1 country
1
Brief Summary
The purpose of the study is to investigate the Comparative Efficacy of Magnesium Sulfate Iontophoresis and Extracorporeal shockwave therapy on Chronic Mechanical Neck Pain
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jun 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 11, 2025
CompletedFirst Posted
Study publicly available on registry
June 18, 2025
CompletedStudy Start
First participant enrolled
June 20, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2025
CompletedAugust 7, 2025
August 1, 2025
3 months
June 11, 2025
August 6, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
pain pressure threshold
pain pressure threshold will be measured by the pressure algometer
0-4 weeks
Pain intensity
pain intensity will be measured by visual analogue scale
0-4 weeks
Secondary Outcomes (1)
Neck Disability Index
0-4 Weeks
Study Arms (3)
Magnesium Sulfate Iontophoresis group
EXPERIMENTALPatients in this group will receive Magnesium Sulfate Iontophoresis, two sessions per week for four weeks
Shock Wave Therapy group
EXPERIMENTALPatients in this group will receive Shock Wave Therapy, one session per week for four weeks
Control group
PLACEBO COMPARATORPatients in this group will receive stretching and strengthening exercises, two sessions per week for four weeks
Interventions
Magnesium Sulfate iontophoresis utilizing an iontophoretic drug delivery system
Eligibility Criteria
You may qualify if:
- medically competent men and women will be included
- They had chronic MTrPs in the upper trapezius for more than 6 months
- Diagnostic criteria of being a tight band with a palpable nodule and distant pain when subjected to pressure
You may not qualify if:
- subjects with previous neck or shoulder pathology (e.g., fracture, sur¬gery, inflammatory and infectious diseases),
- cervical disc pathology, systemic disorder, fibromyalgia,
- those who underwent physical therapy for at least the previous 3 months
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Physical Therapy
Giza, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer
Study Record Dates
First Submitted
June 11, 2025
First Posted
June 18, 2025
Study Start
June 20, 2025
Primary Completion
September 20, 2025
Study Completion
October 1, 2025
Last Updated
August 7, 2025
Record last verified: 2025-08