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A study to compare the efficacy of ozone injection versus dry needling in muscle pain of lower neck region.

Comparison of efficacy of ozone injection and dry needling in myofascial pain syndrome involving trapezius; a randomised control trial. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024561
Enrollment
42
Registered
2020-04-09
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M791- Myalgia

Interventions

Intervention1: Ozone injection: 8 ml of ozone gas with concentration of 15micro gm/ml at MTrP in affected trapezius, using a 24-gauge, 1.25 inch needle once weekly for 3 weeks. Control Intervention1

Sponsors

ESI Institute of Pain Management
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Symptoms lasting >3 months despite conservative treatments including physiotherapy and medications. 2. Presence of active trigger points in the upper trapezius muscles (at least one). 3. Presence of at least one taut band on manual palpation. 4. NRS score 6 and above.

Exclusion criteria

Exclusion criteria: 1. Presence of any history of cervical radiculopathy or degenerative condition, 2. Presence of any surgery or trauma to the neck during last year, 3. Previous injection for MPS treatment during last 6 months, 4. Confirmed diagnosis of cognitive disorders, fibromyalgia, rheumatoid arthritis, and/or metabolic diseases like hypothyroidism and diabetes mellitus.

Design outcomes

Primary

MeasureTime frame
pain evaluated by the numeric pain rating scaleTimepoint: before the treatment and 4 weeks after the last injection.

Secondary

MeasureTime frame
neck disability index (NDI)Timepoint: before the treatment and 4 weeks after the last injection.;Range of motion (ROM) in neck lateral flexion movement measured using goniometryTimepoint: before the treatment and 4 weeks after the last injection.;Tissue Imaging Score based on gray scale imaging and vibration sonography with colour doppler imagingTimepoint: before the treatment and 4 weeks after the last injection.

Countries

India

Contacts

Public ContactDr Subrata Goswami

ESI Institute of Pain Management

drsgoswami@gmail.com09830430430

Outcome results

None listed

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