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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01140230
Other study ID # Hanna Björnsson study 2
Secondary ID
Status Completed
Phase N/A
First received June 8, 2010
Last updated June 8, 2010
Start date August 2009
Est. completion date May 2010

Study information

Verified date September 2009
Source University Hospital, Linkoeping
Contact n/a
Is FDA regulated No
Health authority Sweden: Institutional Review Board
Study type Observational

Clinical Trial Summary

Few studies are considering acute traumatic rotator cuff tears in previously asymptomatic patients. The purpose of the current study was to investigate if delay of surgery, age at repair and the number of cuff tendons involved affected the structural and clinical outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date May 2010
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender Both
Age group 42 Years to 83 Years
Eligibility Inclusion Criteria:

- significant trauma to the shoulder

- sudden onset of symptoms

- asymptomatic in the shoulder before trauma

- pseudoparalysis in the shoulder after trauma

- full thickness rotator cuff tear of at least one tendon

Exclusion Criteria:

- patients with previous or gradual onset of symptoms in the traumatised shoulder

- partial rotator cuff tear

- displaced fracture

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Linkoeping

References & Publications (2)

Bassett RW, Cofield RH. Acute tears of the rotator cuff. The timing of surgical repair. Clin Orthop Relat Res. 1983 May;(175):18-24. — View Citation

Lähteenmäki R, Lawrence S. Public biotech 2006 - the numbers. Nat Biotechnol. 2007 Jul;25(7):729-37. — View Citation

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