None listed
Conditions
Interventions
Procedure/Surgery : The aim of the present study is to compare the efficacy of pain reduction (amount of pain reduction, pain relief duration) between different total volumes (high volume 10ml, modera
lidocaine , high dose 4mg, moderate dose 2mg, low dose 1mg).
Sponsors
Soon Chun Hyang University Hospital Seoul
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) more than 18 year-old adults (2) shoulder pain developed in hemiplegic side after stroke (within 1 year after storke) (3) pain more severe than 4 out of 10 in Numeric rating scale (4) more than 20 scores in Mini mental state examination (K-MMSE) or obey commend 2 steps possible (5) agree with written consent, actively participate in the clinical study procedure
Exclusion criteria
Exclusion criteria: (1) history of injection in hemiplegic shoulder joint within 6 weeks (2) such as fracture or neuropathic pain to induce hemiplegic shoulder pain (3) history of cervical or shoulder surgery (4) pain or history of disease in unaffected shoulder (5) diagnosis of complex regional pain syndrome in hemiplegic shoulder (6) uncontrolled, severe clinical disease such as cardiovascular, pulmonary, hematologic, kidney disease under the physician's judgment (7) pregnant or breast-feeding (8) uncontrolled psychiatric disease such as depression, obsession, anxiety with appropriate managements (9) history of drug overuse (10) uncontrolled diabetes mellitus
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numeric rating scale | — |
Secondary
| Measure | Time frame |
|---|---|
| range of motion | — |
Countries
Korea, Republic of
Contacts
Public ContactYoon-Hee Choi
Soon Chun Hyang University Hospital Seoul
Outcome results
None listed