Status:
NOT_YET_RECRUITING
Lidocaine Versus Magnesium Sulphate in Management of Myofascial Pain Dysfunction Syndrome
Lead Sponsor:
Misr University for Science and Technology
Conditions:
Myofascial Pain Dysfunction Syndrome
Eligibility:
All Genders
18-55 years
Phase:
PHASE2
Brief Summary
The goal of this clinical trial is to investigate the effectiveness of Magnesium Sulphate in the management of myofascial pain dysfunction syndrome in comparison to Lidocaine and Saline. A total of 7...
Eligibility Criteria
Inclusion
- Age Limitations: Participants must be between 18 and 55 years old.
- Chronic Pain Diagnosis: Individuals must have a diagnosis of chronic myofascial pain dysfunction syndrome (MPDS) affecting the face muscles, neck, shoulder, or upper back for a duration exceeding three months.
- Trigger Point Recognition: Patients must show awareness of their pain when pressure is applied to identified myofascial trigger points, in accordance with established diagnostic guidelines.
- Consent to Participate: Willingness to provide informed consent and engage in all aspects of the study.
Exclusion
- Previous Treatments: A history of receiving dry needling or pulsed radiofrequency therapy, or currently participating in other pain management treatments.
- Recent Injury or Surgery: Any recent trauma, surgical procedures, or infections in the affected area within the past six months.
- Medication Interference: Current or recent use of moderate to strong analgesics (e.g., tramadol, morphine) that could influence pain assessment.
- Severe Health Conditions: Individuals with significant systemic illnesses (e.g., severe liver or kidney disease), blood clotting disorders, rheumatoid arthritis or epilepsy.
- Mental Health: Presence of current psychiatric disorders, cognitive impairments, or inability to comply with the study protocol.
Key Trial Info
Start Date :
October 1 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 30 2025
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT06595017
Start Date
October 1 2024
End Date
November 30 2025
Last Update
September 19 2024
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