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Clinical Trials/NL-OMON34278
NL-OMON34278
Completed
Phase 3

Efficacy of post-operative pain management with intralesional ropivacaine after subacromial decompression - Pain management after subacromial decompression.

Ziekenhuisgroep Twente0 sites189 target enrollmentTBD
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Conditionsnot enough space in the shouldersubacromial impingement1000595910005944

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
not enough space in the shoulder
Sponsor
Ziekenhuisgroep Twente
Enrollment
189
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Sponsor
Ziekenhuisgroep Twente

Eligibility Criteria

Inclusion Criteria

  • •Patients (18 years and older) with subacromial impingement syndrome who need a subacromial decompression by dr. C. van Doorn

Exclusion Criteria

  • •Significant damage at the affected shoulder or untreatable subacromial impingement
  • •a history of injury at the affected shoulder
  • •a history of surgery at the affected shoulder
  • •a history of mastectomy at the affected side
  • •a neuropathologic condition at the affected shoulder
  • •chonic use of opioids
  • •extraordinary risk\-increasing factors, like morbid obesity
  • •Parkinsons disease
  • •contraindications for the used medications
  • •disability which leads to an inability to describe pain and inability to fill in the VAS score.

Outcomes

Primary Outcomes

Not specified

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