adhesive capsulitis
Conditions
Interventions
control group:sedation and analgesia for manual release
Experimental group:Silver needle pre release combined with sedation and analgesia for manual release
Sponsors
Xiamen Medical University Affiliated Second Hospital
Eligibility
Sex/Gender
All
Age
45 Years to 70 Years
Inclusion criteria
Inclusion criteria: Age Range: Participants must be between 45 and 70 years of age. Duration of Symptoms: The duration of shoulder pain or stiffness must be more than 1 month. Absence of Severe Underlying Diseases: No history of severe cardiac disease. No history of neurological disorders. No history of coagulation dysfunction or other relevant hematological disorders. Voluntary Participation and Informed Consent: Participants must voluntarily agree to participate in the study and sign an informed consent form indicating their understanding of the study's objectives procedures potential risks and benefits.
Exclusion criteria
Exclusion criteria: (1) shoulder joint X-ray examination excludes patients with shoulder fractures and dislocations MRI examination excludes patients with rotator cuff injuries of grade three or above and excludes patients with tendon ruptures; (2) Patients who have received invasive treatment for other shoulder injuries within the past half month; (3) Shoulder pain caused by other reasons; (4) Patients with local skin infections in the treatment area as well as those with hematological and psychiatric disorders who cannot cooperate with treatment and have contraindications for invasive procedures
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| range of motion;NRS; | — |
Secondary
| Measure | Time frame |
|---|---|
| Medication;Sleep rating; | — |
Countries
China
Contacts
Public ContactGuanghui Zhang
Xiamen Medical University Affiliated Second Hospital
Outcome results
None listed