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Clinical Trials/ITMCTR2000003732
ITMCTR2000003732Not yet recruitingPhase 1

Study on Ultrasonic Visualization and Standardization of Acupuncture Treatment of Neck, Shoulder and Low Back Pain

Shanghai Municipal Hospital of Traditional Chinese Medicine0 sitesStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 1
Status
Not yet recruiting

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional study

Eligibility Criteria

Ages
35 to 60 (—)
Sex
All

Inclusion Criteria

  • (1) Patients whose clinical diagnosis meets the diagnostic criteria of vertebral artery type cervical spondylosis, periarthritis, and acute lumbar sprain;
  • (2) Aged 35-60 years, no gender limit;
  • (3) If CSA patients undergo conservative treatment, a 5-day washout period is required;
  • (4) Patients with acute lumbar sprain must have the first onset and the course of disease is less than 5 days;
  • (5) The active or passive movement of patients with frozen shoulder is restricted, and the course of disease is 6 weeks to 6 months;
  • (5) Those who have not participated in other studies within 6 months before entering the study;
  • (7) Patients who participate voluntarily, understand and sign informed consent.

Exclusion Criteria

  • (1) Those who with blood, infection and severe osteoporosis diseases;
  • (2) Those who have serious basic diseases such as heart, lung, and brain;
  • (3) Patients who have been diagnosed with mental illness;
  • (4) Patients who have recently become pregnant or are pregnant or breastfeeding;
  • (5) The history of trauma, fracture, surgery, tumor and other diseases of the neck, waist, shoulder and other parts should be excluded;
  • (6) Exclude patients who use non-steroidal anti-inflammatory drugs or analgesics;
  • (7) Patients with frozen shoulder should exclude dislocations and rotator cuff tears; superior nerve compression syndrome, shoulder-hand syndrome, thoracic outlet syndrome, brachial plexus neuritis and other peripheral nerve diseases that cause shoulder pain;
  • (8) Those whose relevant imaging studies do not meet the inclusion criteria;
  • (9) Patients who refuse to accept ultrasound-guided acupuncture.

Investigators

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