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Clinical study of acupotome treatment of refractory non-specific low back pain based on the theory of "regulation and balance"

Clinical Observation on Treatment of refractory non-specific low back pain with Needle-Knife release therapy based on the "regulation and balance theory"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000200
Enrollment
Unknown
Registered
2024-08-09
Start date
2023-03-01
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

refractory non-specific low back pain

Interventions

control group:usual care
observation group:Musculoskeletal ultrasound-guided Needle-Knife release therapy

Sponsors

Longhua Hospital, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) The patient can cooperate with treatment and has no cognitive dysfunction; 2) Consistent with the diagnosis of chronic non-specific low back pain; 3) The duration of low back pain =12 months, repeated or continuous pain =6 months; 4) Received =90 days of medical intervention (including drug and non-drug therapies); 5) NRS score 4-8 (0-10); 6) ODI score 13-36 (on a scale of 0 to 50); 7) Lumbar segmental stability test in prone position was positive; 8) No treatment related to refractory non-specific low back pain was performed in the 2 weeks prior to the study; 9) Signed informed consent, subjects have good compliance, voluntarily participate in this study, and are willing to accept examination, treatment and follow-up follow-up.

Exclusion criteria

Exclusion criteria: 1) Suffering from specific low back pain diseases: spinal disorders, neurological disorders, visceral system disorders, vascular disorders, psychogenic disorders and other factors; 2) Combined with mental illness, speech and/or cognitive impairment, unable to actively cooperate with treatment and follow-up; 3) Previous low back surgery history; 4) Patients who take drugs that affect the efficacy for a long time; 5) Pregnant and lactating women; 6) The surgical site is damaged and seriously infected; 7) Allergic to anesthetic drugs such as lidocaine hydrochloride.

Design outcomes

Primary

MeasureTime frame
Numerical rating scale;—

Secondary

MeasureTime frame
Oswestry disability index;Japanese Orthopaedic Association Scores;4th lumba multifidus muscle thickness;—

Countries

China

Contacts

Public ContactZhanying Tang

Longhua Hospital, Shanghai University of Traditional Chinese Medicine

tzy79@126.com13585622728

Outcome results

None listed

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