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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01242761
Other study ID # 0092-10-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received November 16, 2010
Last updated November 16, 2010
Start date January 2011
Est. completion date January 2012

Study information

Verified date November 2010
Source Hillel Yaffe Medical Center
Contact Gil Laufer, MD
Phone 972-4-630-4160
Email GilL@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

After comparing ultrasound study of rotator cuff injuries that have been evaluated both in the community and in a hospital-based ultrasound service with actual surgical findings, it is expected that specialist performed imaging and evaluation will be most accurate and that those performed in the community will be not accurate enough.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date January 2012
Est. primary completion date January 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Symptomatic rotator cuff tears Indication for rotator cuff repair

Exclusion Criteria:

- Severe arm movement limitations

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rotator cuff tear surgical findings more accurately reflect hospital-based US imaging findings One year No
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