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Clinical Trials/ITMCTR2024000200
ITMCTR2024000200
Completed
未知

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

onghua Hospital, Shanghai University of Traditional Chinese Medicine0 sitesTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
onghua Hospital, Shanghai University of Traditional Chinese Medicine
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional study
Sex
All

Investigators

Sponsor
onghua Hospital, Shanghai University of Traditional Chinese Medicine

Eligibility 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

  • 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.

Outcomes

Primary Outcomes

Not specified

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