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Arthroscopic Versus Open Stabilization for Traumatic Shoulder Instability
This study is ongoing, but not recruiting participants.
Study NCT00251264   Information provided by University of Calgary
First Received: November 8, 2005   Last Updated: February 17, 2009   History of Changes

November 8, 2005
February 17, 2009
November 2001
February 2011   (final data collection date for primary outcome measure)
Western Ontario Shoulder Instability (WOSI) Index [ Time Frame: Baseline, 3, 6, 12, 24 months post-operatively ] [ Designated as safety issue: No ]
Western Ontario Shoulder Instability (WOSI) Index
Complete list of historical versions of study NCT00251264 on ClinicalTrials.gov Archive Site
  • American Shoulder and Elbow Society (ASES) score [ Time Frame: Baseline, 3, 6, 12, 24 months post-operatively ] [ Designated as safety issue: No ]
  • Physical examination: range of motion, strength, stability [ Time Frame: Baseline, 3, 6, 12, 24 months post-operatively ] [ Designated as safety issue: No ]
  • Return to sport or activity, return to work [ Time Frame: Baseline, 3, 6, 12, 24 months post-operatively ] [ Designated as safety issue: No ]
  • Complications [ Time Frame: Intra-operatively and up to 2 weeks post-operatively ] [ Designated as safety issue: No ]
  • Time to perform each procedure [ Time Frame: Day of surgery ] [ Designated as safety issue: No ]
  • Economic cost of each procedure [ Time Frame: Day of surgery ] [ Designated as safety issue: No ]
  • American Shoulder and Elbow Society (ASES) score
  • Physical examination: range of motion, strength, stability
  • Return to sport or activity, return to work
  • Complications
  • Time to perform each procedure
  • Economic cost of each procedure
 
Arthroscopic Versus Open Stabilization for Traumatic Shoulder Instability
Arthroscopic Versus Open Stabilization of Traumatic Unidirectional Anterior Shoulder Instability: A Randomized Clinical Trial

The purpose of this study is to compare arthroscopic and open shoulder stabilization procedures by measuring the disease-specific quality of life outcome in patients with traumatic unidirectional anterior instability of the shoulder at 2 and 5 years.

Hypothesis: There is no difference in disease-specific quality of life outcomes in patients with traumatic unidirectional anterior shoulder instability, undergoing an arthroscopic versus an open stabilization procedure.

Shoulder instability most commonly affects people in the late teens to mid thirties, which are the most active years, recreational and vocational. The resulting disability, time lost from work, as well as the effect on an individual's quality of life represent a significant clinical problem for the population and for the healthcare system.

The normal anatomy in the unstable shoulder can be restored using arthroscopic or open surgical stabilization techniques. There is considerable controversy surrounding the issue of arthroscopic versus open shoulder stabilization. Advocates of arthroscopic procedures cite the following as advantages: faster recovery, less post operative pain, decreased operative time, improved cosmetics, greater return of shoulder motion and the more accurate identification of intraarticular pathology. Those in favor of an open procedure cite superior long term results showing fewer recurrences with an open stabilization.

There are few published reports directly comparing arthroscopic versus open shoulder stabilization repairs. It is also difficult to compare the results of existing studies as they report on heterogeneous patient populations, using a variety of techniques on mixed pathologies, using different outcome scales and variable definitions of success and failure. This study will address this controversial issue by comparing the disease-specific quality of life outcomes in patients with traumatic unidirectional anterior shoulder instability undergoing an arthroscopic versus an open stabilization procedure.

This study is designed as a prospective randomized clinical trial with a second prospective analytical cohort study arm. In the randomized arm, patients are assigned to arthroscopic or open surgery based on varied block, computer-generated randomization. The expertise-based randomization method is used in this study, whereby the surgeons perform either arthroscopic or open surgery, but not both. Therefore, a patient is not only randomized to a treatment group, but is also assigned to the expert surgeon for that treatment.

Patients in the prospective analytical cohort study arm of the trial undergo shoulder stabilization (open or arthroscopic) with any surgeon and complete the same follow-up visits, however they have not been randomized. The outcomes of the prospective cohort will be compared to those of the randomized arm to determine if the expertise-based randomization method has an effect on patient outcome.

Disease-specific quality of life is assessed using the validated Western Ontario Shoulder Instability (WOSI) Index. The index has 21 questions divided into 4 categories: physical symptoms, sport/recreation/work, lifestyle and emotions. This self-administered questionnaire utilizes a 100mm visual analog scale format to provide an overall score out of 100. A lower score reflects a better quality of life.

 
Interventional
Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Efficacy Study
  • Joint Instability
  • Shoulder Dislocation
  • Procedure: Open stabilization
  • Procedure: Arthroscopic stabilization
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
194
February 2011
February 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Clinical:

    • Age 14 years or greater
    • Diagnosis of traumatic anterior shoulder instability, made by meeting all of the following:

      1. Radiographic evidence or documented physician assisted reduction of anterior shoulder dislocation following a traumatic injury.
      2. Ability to elicit unwanted glenohumeral translation which reproduce symptoms with one of the following tests: anterior apprehension, relocation test, or anterior load and shift test
  • Radiological:

    • Closed growth plate on a standardized series of x-rays consisting of a minimum of an anteroposterior view, lateral in the scapular plane and an axillary view.

Exclusion Criteria:

  • Clinical:

    • Diagnosis of multidirectional instability (MDI) or multidirectional laxity with anteroinferior instability (MDL-AII), made by two or more of:

      1. Symptomatic (pain or discomfort) in inferior or posterior direction
      2. Ability to elicit unwanted posterior glenohumeral translation that reproduces symptoms with posterior apprehension tests, or posterior load and shift test
      3. Positive sulcus sign of 1cm or greater that reproduces patient's clinical symptoms
    • Previous surgery on the affected shoulder other than diagnostic arthroscopy
    • Cases involving litigation
    • Significant tenderness of acromioclavicular/sternoclavicular joints on affected side
    • Confirmed connective tissue disorder (ie: Ehlers-Danlos, Marfan)
Both
14 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT00251264
Denise Chan, Orthopaedic Research Coordinator, University of Calgary
15740
University of Calgary
  • Calgary Health Region
  • Calgary Orthopaedic Research and Education Fund (COREF)
  • Hip Hip Hooray
Principal Investigator: Nicholas Mohtadi, MD, FRCSC University of Calgary Sport Medicine Centre
Principal Investigator: Robert Hollinshead, MD, FRCSC University of Calgary Sport Medicine Centre
University of Calgary
February 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP