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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00589433
Other study ID # SAF02-HMO-CTIL
Secondary ID
Status Terminated
Phase N/A
First received January 1, 2008
Last updated March 21, 2013

Study information

Verified date March 2013
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Rotator culf tears are common in the aging population and are a significant morbidity source. The common knowledge is that the major tears do not heal and constantly expanding.Still since the majority of the patients are old the acceptable therapy is conservative treatment.

Our objective is to estimate the accuracy of rotator culf tear utilizing an ultrasound.


Recruitment information / eligibility

Status Terminated
Enrollment 50
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 35 Years to 65 Years
Eligibility Inclusion Criteria:

- Was diagnosed with shoulder tear

- Size of the tear till 2.5 cm

- The opposite tendon-normal

Exclusion Criteria:

- systematic Diseases .

- Injury to the shoulder after the previous US.

- Pregnancy

Study Design

Observational Model: Case-Crossover, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Hadassah Orthopedic Department Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel,