None listed
Conditions
Interventions
Drug : ? experimental group : intra-articular triamcinolone injection (sono guided), 4 weeks interval, maximal twice
(dose : 40mg triamcinolone (if, DM patients : 20mg)
? control group : PO solondo
Sponsors
National Rehabilitation Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patients with CRPS diagnosed by Budapest criteria Hemiplegic patients aged 19 and over with limited lesions to one side primary stroke patients with congtivie ability to understand and follow the researchers' instructions persons who have understood the contents of this research experiment and have agreed to participate by themselves or their guardians
Exclusion criteria
Exclusion criteria: patients with fracture of the hemiplegic upper extremity or undergoing orthopedic surgery patients with unregulated diabetes or type 1 diabetes those who are restricted from using steroids uncontrolled hypertension pregnant woman patients with bacterial infection patients with blood clotting disorder (coagulopathy) patients with damage to the skin of the injection area patients who have been injected with steroids in the shoulder joint within one month patients who have been injected in the shoulder joint within three months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS for shoulder pain in the affected limb (0-10 cm) | — |
Secondary
| Measure | Time frame |
|---|---|
| symptom/sensory(hyperesthesia,allodynia) | — |
Countries
Korea, Republic of
Contacts
Public ContactEun Young Kim
National Rehabilitation Hospital
Outcome results
None listed