hemiplegic shoulder pain
Conditions
Interventions
group of acupoint catgut embedding:Subjects receive acupoint catgut embedding at Jianyu point (LI15), Quchi point (LI1), Shoulder Zhen point (SI9) and shoulder Liao point (SJ14) on the affected side.
group of radiofrequency ablation around shoulder trigger points:Subjectes receive radiofrequency ablation to trigger points around the troubled side shoudler
Group of acupoint catgut embedding combined with radiofrequency ablation to trigger points around the troubled shoudler:Subjects Receive acupoint catgut embedding combined with radiofrequency ablatio
Sponsors
Shanghai Fourth People's Hospital affiliated to Tongji University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1)Meet stroke diagnostic criteria, 14 days to 12 months after the onset of stroke; 2) Shoulder pain occurs after stroke; 2) The NRS score of hemiplegic shoulder pain in resting state was 1-8 points, and the NRS4-10 points of active-induced shoulder pain; 3) The patient had not received any treatment for shoulder pain or participated in other clinical trials at least 1 week before the study; 4) Age over 18 years old, gender is not limited; 5) The participants had stable vital signs, clear consciousness, good cognitive ability, and the ability to follow orders at least 48 hours before the study; 6) The patient signed the informed consent voluntarily.
Exclusion criteria
Exclusion criteria: 1) Participants inobservance or unwilling to the study; 2) Shoulder pain occurs before stroke and caused by other diseases (such as cervical spondylosis, periarthritis of shoulder, rotator cuff injury); Or shoulder pain caused by damage to the thalamus; 3) Severe liver and kidney dysfunction or heart function of grade 3 or above; 4) Mental disorder or disturbance of consciousness; 5) Fear of acupuncture or dizziness; The skin at the buried acupuncture point is damaged or infected, and the radio frequency is contraindicated (coagulation dysfunction, pacemaker implantation, and vital signs are unstable).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl-Meyer upper limb mobility strength score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pittsburgh Sleep Scale score;Hamilton anxiety and depression score;SF-36 Life Scale score;Name, dosage of pain relievers taken by patients during the study period (as prescribed in the doctor's order and self-administered);Complications associated with embedding and radiofrequency during the study;Duration of complete cessation of recovery during patient follow-up; | — |
Countries
China
Contacts
Public ContactChen Hui
Shanghai Fourth People's Hospital affiliated to Tongji University
Outcome results
None listed