Patients with type I CPRS after stroke
Conditions
Interventions
Experimental group:Applying stellate ganglion block combined with iTBS on the basis of the control group
Sponsors
Shandong Provincial Third Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1.The diagnosis complies with the "Stroke Diagnosis Criteria" in the "Chinese Guidelines and Consensus for the Diagnosis and Treatment of Cerebrovascular Diseases (2016 Edition)", and the lesion site has been confirmed by cranial CT or MRI; 2.The age is between 18 and 70 years old; 3.The affected side of the upper limb experiences pain, and it conforms to the newly revised Budapest (Budapest) criteria in 2010; 4.Other drug treatments have not been effective; 5.The patient consents voluntarily, the family is informed, and the informed consent form is signed.
Exclusion criteria
Exclusion criteria: 1.Those who already have diseases such as peripheral nerve damage, shoulder arthritis, rotator cuff injury, shoulder joint fractures, and rheumatoid arthritis that affect the upper limb's movement function before the stroke; 2.Patients with unstable conditions or those with severe physical diseases; ? Those with cognitive dysfunction; 3.Those with cognitive dysfunction; 4.Those currently taking drugs for neuropathic pain treatment; 5.Those with intracranial metal foreign bodies or with implanted cardiac pacemakers, heart stents, cochlear implants, increased intracranial pressure, having had epileptic seizures or a family history of epilepsy; 6.Those with severe mental disorders or other reasons that prevent cooperation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Simplified McGill Pain Questionnaire; | — |
Secondary
| Measure | Time frame |
|---|---|
| Functional Magnetic Resonance Imaging;Fugl-Meyer assessment scale;Motor Function Status Scal;Improved Barthel Index;Blood factors; | — |
Countries
China
Contacts
Public ContactBo Zhihui
Shandong Provincial Third Hospital
Outcome results
None listed