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Clinical Trials/ACTRN12613000569707
ACTRN12613000569707
Completed
未知

In individuals undergoing shoulder, hip and knee arthroscopy, how does the use of ArthroCare 'Coblation technology' ablation system compare to the regular diathermy ablation system effect in the intra-articular fluid temperatures during arthroscopy?

ORIQL (Orthopaedic Research Institute of Queensland)0 sites80 target enrollmentMay 20, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Shoulder Arthroscopy
Sponsor
ORIQL (Orthopaedic Research Institute of Queensland)
Enrollment
80
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 20, 2013
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
ORIQL (Orthopaedic Research Institute of Queensland)

Eligibility Criteria

Inclusion Criteria

  • 1\) Clinically indicated for shoulder arthrosopcy:
  • \- rotator cuff repair
  • \- sub\-acromial decompression, acromioplasty
  • \- acromioclavicular joint excision
  • \- shoulder stabilisation or labral repair
  • 2\) Clinically indicated for knee arthroscopy
  • \- ACL reconstruction
  • 3\) Hip arhtroscopy for femoral acetabular impingement

Exclusion Criteria

  • \<18 years of age

Outcomes

Primary Outcomes

Not specified

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