SSNB in Hemiplegic Shoulder Pain
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Purpose
The purpose of this study is to compare suprascapular nerve block with therapeutic ultrasound in stroke patients who have shoulder pain in weak side.
| Condition | Intervention | Phase |
|---|---|---|
|
Shoulder Pain Stroke |
Drug: 1% xylocaine Other: ultrasound |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Suprascapular Nerve Block in Hemiplegic Shoulder Pain. |
- VAS score of pain [ Time Frame: 4 weeks after intervention ] [ Designated as safety issue: No ]
- Range of motion of the shoulder joint [ Time Frame: 4 weeks after intervention ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 0 |
| Study Start Date: | August 2008 |
| Study Completion Date: | May 2009 |
| Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: A
Suprascapular nerve block
|
Drug: 1% xylocaine
10 cc. of 1%xylocaine, once a week
Other Name: suprascapular nerve block
|
|
Experimental: B
therapeutic ultrasound
|
Other: ultrasound
ultrasound at shoulder area about 10 mins.
Other Name: therapeutic ultrasound
|
Detailed Description:
Shoulder pain is a common complication after a cerebrovascular accident.Hemiplegic shoulder pain has been shown to affect stroke outcome in a negative way.It interferes with recovery after stroke:it can cause distress and reduced activities and can markedly hinder rehabilitation.Suprascapular nerve block has been shown to be effective as an analgesic for different indications such as shoulder capsulitis.The purpose of this study was to evaluate the effectiveness of this technique conjunction with a rehabilitation program to reduce shoulder pain in hemiplegic patients.
Eligibility| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Stroke patients who develope shoulder pain at weak limb.
- Good conscious and able to access pain score.
- No history of drug reaction with xylocaine
- No history of fracture,tumor or blood tendency.
- Willing to enrolled to study and signs inform consent.
Exclusion Criteria:
- Patients who do not meet the inclusion criteria.
Contacts and Locations| Thailand | |
| Department of physical medicine and rehabilitation, Faculty of medicien, Chulalongkorn University | |
| Bangkok, Thailand | |
| Principal Investigator: | Jariya Boonhong, physiatist | Unaffiliation |
More Information
No publications provided
| Responsible Party: | Jariya Boonhong/ Department of Rehabilitation Medicine, Faculty of Medicine, Chulalongkorn University, Chulalongkorn University |
| ClinicalTrials.gov Identifier: | NCT00732589 History of Changes |
| Other Study ID Numbers: | Chulalongkorn University |
| Study First Received: | August 8, 2008 |
| Last Updated: | November 17, 2009 |
| Health Authority: | Thailand: Food and Drug Administration |
Keywords provided by Chulalongkorn University:
|
suprascapular nerve block shoulder pain hemiplegia |
Additional relevant MeSH terms:
|
Shoulder Pain Stroke Arthralgia Joint Diseases Musculoskeletal Diseases Pain Signs and Symptoms Cerebrovascular Disorders Brain Diseases Central Nervous System Diseases Nervous System Diseases Vascular Diseases Cardiovascular Diseases |
Lidocaine Anesthetics, Local Anesthetics Central Nervous System Depressants Physiological Effects of Drugs Pharmacologic Actions Sensory System Agents Peripheral Nervous System Agents Central Nervous System Agents Therapeutic Uses Anti-Arrhythmia Agents Cardiovascular Agents |
ClinicalTrials.gov processed this record on May 16, 2013