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Comparison of the Efficacy of Dry Needling and Intradermal Needling in the Treatment of Lumbar Muscle Strain: A Randomized Controlled Trial

Comparison of the Efficacy of Dry Needling and Intradermal Needling in the Treatment of Lumbar Muscle Strain: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000061
Enrollment
Unknown
Registered
2026-01-13
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

lumbar muscle strain

Interventions

DN:Acupoint location: Based on palpation, identify 2-4 most prominent myofascial trigger points (MTrPs) in the painful area of the lumbar and dorsal regions (such as erector spinae, quadratus lumborum
ITN:Acupuncture point selection/positioning: The same as the DN group, the same anatomical area and muscle groups were chosen. * Procedure: Use a dedicated internal heat needle device and disposable

Sponsors

Jiaxing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: * Age: 18 to 65 years old; * Meeting the above Western medical diagnostic criteria; * Visual Analogue Scale (VAS) for pain = 4 points; * Voluntarily participating in this study and signing the informed consent form.

Exclusion criteria

Exclusion criteria: * Presence of definite radicular symptoms (such as positive straight leg raising test with radiating pain) or specific causes of low back pain (such as lumbar intervertebral disc protrusion, vertebral fractures, tumors, infections, inflammatory diseases, rheumatic immune diseases, severe osteoporosis); * Previous history of lumbar spine surgery; * Concurrent severe primary diseases of the heart, brain, liver, kidneys, etc. or mental disorders; * Coagulation disorders or currently taking anticoagulant drugs; * Skin damage, infection or sensory disorders at the acupuncture site; * Pregnant or lactating women; * Extreme fear or allergy to acupuncture or heat stimulation; * Received other systemic acupuncture, massage or physical therapy within the past month; * Unable to complete the questionnaire or comply with the research protocol.

Design outcomes

Primary

MeasureTime frame
VAS;

Secondary

MeasureTime frame
Oswestry Disability Index;Roland-Morris DisabilityQuestionnaire,RMDQ;SF-36 Health Survey Short Form;Clinical Global Impression-Improvement Scale (CGI-I) ;spinal mobility;Analgesic dosage;

Countries

China

Contacts

Public ContactHaojia Li

Jiaxing First Hospital

declanhaojia@163.com18435148486

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026