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Clinical Trials/NL-OMON47590
NL-OMON47590
Withdrawn
Not Applicable

Central pain sensitisation or (peri)articular damage: the origin of pain in SAPS A randomised, placebo controlled, blinded, cross-over trial - PARTItrial

eids Universitair Medisch Centrum0 sites40 target enrollmentTBD
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ConditionsChronische pijn in de schouderPainful Arc SyndromeSubacromial Impingement Syndrome10013361

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronische pijn in de schouder
Sponsor
eids Universitair Medisch Centrum
Enrollment
40
Status
Withdrawn
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • •\- Chronic shoulder pain (\>3 months)
  • •\- Unilateral shoulder pain
  • •\- Suspicion of subacromial origin of pain (e.g. positive painful arc test, Hawkins\-Kennedy test, empty can test)
  • •\- Presence of conventional ultrasonography
  • •\- Presence of conventional radiographs

Exclusion Criteria

  • •\- Younger than 18 years of age
  • •\- Tendinitis calcarea
  • •\- Full thickness rotator cuff tear
  • •\- Suspicion of capsulitis adhesiva after clinical examination
  • •\- Glenohumeral osteoarthritis
  • •\- Medication that potentially act on central pain sensitisation (e.g. pregabalin, amitriptylin, duloxetine)
  • •\- Use of opioid analgesics, e.g. oxycodone.
  • •\- Suspicion of symptomatic acromioclavicular osteoarthritis (e.g. positive cross body adduction test)
  • •\- History of fractures or dislocations of the shoulder
  • •\- Cardiac disease

Outcomes

Primary Outcomes

Not specified

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