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Comparing the effect of ketorolac mesotherapy versus methylprednisolone injection in trigger points in reducing pain and improving performance in patients with lumbosacral canal stenosis

Comparing the effect of ketorolac mesotherapy versus methylprednisolone injection in trigger points in reducing pain and improving performance in patients with lumbosacral canal stenosis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250530065985N1
Enrollment
72
Registered
2025-07-05
Start date
2025-09-23
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

lumbosacral canal stenosis. Spinal stenosis, lumbar region

Interventions

Intervention 1: Intervention group: Ketorolac injection by mesotherapy method. Intervention 2: Intervention group: Injection of methylprednisolone into trigger points.

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria are: completion and signing of the informed consent form, presence of pain and other clinical symptoms of lumbosacral spinal stenosis L4-L5-S1 (confirmed by paraclinical tests MRI and nerve and muscle conduction study) in the past six months and lack of response to conservative treatments, age between 35-75 years, and absence of any disease around the spine.

Exclusion criteria

Exclusion criteria: Exclusion criteria are: diabetes mellitus, rheumatic and collagen vascular diseases, gout and lupus, nerve damage and neuropathies, brucellosis, body mass index above 41, history of spinal trauma and fracture, presence of emergency surgical criteria for the spine (red flag), bleeding disorders, inability to communicate and complete questionnaires, history of allergy and hypersensitivity reactions to the drugs used, history of significant liver, kidney, and cardiopulmonary disorders, history of injections into or around the spine in the past 3 months, pregnancy, individuals with cancer, and individuals currently using anticoagulant medications.

Design outcomes

Primary

MeasureTime frame
Pain relief. Timepoint: Weeks 2, 4 and 8 after the last treatment session. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Functional improvement. Timepoint: Weeks 2, 4 and 8 after the last treatment session. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Reza Farpoor

Shiraz University of Medical Sciences

farporh@sums.ac.ir+98 71 3230 5410

Outcome results

None listed

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