Complex regional pain syndrome
Conditions
Interventions
experimental group:routine rehabilitation+MLD+rTMS
control group:routine rehabilitation
Sponsors
north branch of Huashan Hospital, Fudan University
Eligibility
Sex/Gender
All
Age
40 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Aged 40 to 80 years, male or female; 2. According to the "Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke in China" (2014 edition), diagnosed as cerebral infarction; diagnosed as cerebral hemorrhage according to "Guidelines for the diagnosis and treatment of Chinese cerebral hemorrhage" (2014 edition); 3. Comply with the CRPS diagnostic criteria proposed by the IASP (Budapest standard); 4. CRPS classification is type I (without peripheral nerve injury); 5. CRPS progress period: within 6 months; 6. The vital signs are stable, without serious speech and cognitive impairments, which can be easily communicated and can be combined with rehabilitation therapy; 7. Voluntary signing of informed consent and willingness to participate in this study.
Exclusion criteria
Exclusion criteria: 1. Peripheral nerve injury or disease history; 2. History of external injuries, fractures, and muscle tendon injuries in the affected limbs; 3. Limb thrombosis on the affected side; 4. History of rheumatic diseases; 5. Serious infections such as erysipelas; 6. Severe cardiovascular, respiratory, liver and kidney diseases, unstable clinical symptoms; 7. History of tumor disease; 8. Severe malnutrition; 9. There are contraindications for MLD and rTMS; 10. Participating in other relevant clinical researchers at the same time; 11. Pregnant.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hand volume;Degree of pain;motor function;mental status; | — |
Countries
China
Contacts
Public ContactBai Yulong, Qiu Xiao
Huashan Hospital, Fudan University
Outcome results
None listed