Study on the Visualization and Standardization of Acupuncture Technology Guided by Ultrasound

Phase 1

Recruiting

Conditions: Cervical spondylosis of vertebral artery type, frozen shoulder\ acute lumbar sprain pain

Registration Number: ITMCTR2000003787

Lead Sponsor: Shanghai Municipal Hospital of Traditional Chinese Medicine

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: All

Target Recruitment: Not specified

Inclusion Criteria

(1) Patients whose clinical diagnosis meets the diagnostic criteria of vertebral artery type cervical spondylosis, periarthritis, and acute lumbar sprain;
(2) 35-60 years old, 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;
(6) Those who have not participated in other studies within 3 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.

Study & Design

Study Type: Interventional study

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Response rate;

Secondary Outcome Measures

Name	Time	Method
ROM;Constant;Transcranial Doppler, TCD;Infrared imaging technology;Points evaluation;VAS;Clinical evaluation scale of doctor's acupuncture sensation;Clinical evaluation scale of subject's acupuncture sensation;