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Treating painful spots in the upper trapezius muscle with two mesotherapy treatment protocols

Studying the effect and comparison of two mesotherapy treatment protocols for improving clinical symptoms in patients with painful points in the upper trapezius muscle: A randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221108056446N13
Enrollment
52
Registered
2025-01-19
Start date
2025-02-19
Completion date
Unknown
Last updated
2025-02-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain in the upper trapezius muscle. Chronic pain syndrome

Interventions

Intervention 1: Intervention group: In addition to standard and routine treatment, the patient receives 4 subcutaneous injection sessions (including 20 mg of piroxicam in a volume of 1 ml + 1 ml of 2%

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Visual analog scale greater than 5 Pain duration greater than two months Patients who have received standard treatment and have not improved after one month Patient consent to participate in the study

Exclusion criteria

Exclusion criteria: History of cervical spine fracture and spine-related problems Neck surgery, myelopathy or cervical radiculopathy after patient examination Patients with pain perception and recognition disorders Patients with known myopathy and polyneuropathy Mental illnesses or cognitive disorders Drug addiction Receiving narcotics and corticosteroids orally or intravenously in the last 6 months Pregnancy and blood clotting problems Patient's failure to return for follow-up Worsening or exacerbation of the patient's symptoms to the point where other treatment is required Patient's unwillingness to continue treatment or participate in the study

Design outcomes

Primary

MeasureTime frame
Pain reduction in the patient. Timepoint: before the treatment, immediately after the treatment, one month and three months after the treatment in each of the two groups. Method of measurement: VAS pain scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Taheri

Esfahan University of Medical Sciences

PRS_TAHERI@YAHOO.COM+98 913 101 3581

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026