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The origin of pain in the Subacromial Pain Syndrome.

Recruiting
Conditions
Subacromial Pain Syndrome
Subacromial Impingement Syndrome
chronic shoulder pain.
Registration Number
NL-OMON26751
Lead Sponsor
eiden University Medical Center (LUMC)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

Chronic shoulder pain (>3 months)

- Unilateral shoulder pain

Exclusion Criteria

- Younger than 18 years of age

- Tendinitis calcarea

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1) (peri)articular pain determined from effect of subacromial injections on pain at rest and during abduction assessed with a visual analogue scale (VAS), 2) pain sensitisation assessed with bilateral Quantitative Sensory Testing (QST), 3) shoulder muscle activation (expressed as Activation Ratios, ARs).
Secondary Outcome Measures
NameTimeMethod
Secondary study parameters (determinants) are two anchor questions for pain, findings from ultrasonography, questionnaires and demographics.
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