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Clinical Trials/NCT00732589
NCT00732589
Completed
Phase 2

Suprascapular Nerve Block in Hemiplegic Shoulder Pain.

Chulalongkorn University1 site in 1 countryAugust 2008

Overview

Phase
Phase 2
Intervention
1% xylocaine
Conditions
Shoulder Pain
Sponsor
Chulalongkorn University
Locations
1
Primary Endpoint
VAS score of pain
Status
Completed
Last Updated
16 years ago

Overview

Brief Summary

The purpose of this study is to compare suprascapular nerve block with therapeutic ultrasound in stroke patients who have shoulder pain in weak side.

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.

Registry
clinicaltrials.gov
Start Date
August 2008
End Date
May 2009
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Eligibility Criteria

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.

Arms & Interventions

A

Suprascapular nerve block

Intervention: 1% xylocaine

B

therapeutic ultrasound

Intervention: ultrasound

Outcomes

Primary Outcomes

VAS score of pain

Time Frame: 4 weeks after intervention

Secondary Outcomes

  • Range of motion of the shoulder joint(4 weeks after intervention)

Study Sites (1)

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