Imaging of Soft Tissues

This study has been completed.
Sponsor:
Information provided by:
University of Michigan
ClinicalTrials.gov Identifier:
NCT00796094
First received: November 21, 2008
Last updated: November 24, 2009
Last verified: November 2009
  Purpose

The purpose of this study is to evaluate the potential importance of tissue elasticity in the assessment of soft tissues including muscles, tendons and ligaments and other soft tissue structures.

The evaluation of tissue elasticity (easily stretched or moveable) may assist in assessment of various soft tissue structures, such as fatty atrophy of muscles, tendon/ligamentous injury and healing and other soft tissue structures.


Condition Intervention
Soft Tissue Injury
Other: Ultrasound examination

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Elasticity Imaging of Soft Tissues

Further study details as provided by University of Michigan:

Primary Outcome Measures:
  • To assess the potential importance of Sonoelastography in evaluating tissue injury or abnormalities of soft tissues. [ Designated as safety issue: No ]

Estimated Enrollment: 200
Study Start Date: December 2008
Study Completion Date: February 2009
Primary Completion Date: February 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Evaluation of tissue elasticity
Evaluate the potential importance of tissue elasticity in the assessment soft tissue structures.
Other: Ultrasound examination
Sonoelastrography is an ultrasound examination that can determine the elasticity of soft tissue. This examination takes approximately 10 minutes to complete.

Detailed Description:

Stiffness/elasticity of the tissue can be assessed by mechanical excitation with measurement of resultant tissue motion. Reconstruction of the elastic deformability (strain imaging) in real time ultrasound is known as sonoelastography.

Elasticity ultrasound imaging will be performed on the area being evaluated clinically.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Males and non pregnant females with soft tissue abnormalities.

Criteria

Inclusion Criteria:

  • Subjects who present for a clinically ordered ultrasound for evaluation of a soft tissue abnormality.

Exclusion Criteria:

  • Women who are pregnant
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00796094

Locations
United States, Michigan
University of Michigan Hospital
Ann Arbor, Michigan, United States, 48109
Sponsors and Collaborators
University of Michigan
Investigators
Principal Investigator: Yoav Morag, M.D. University of Michigan
  More Information

No publications provided

Responsible Party: Yoav Morag M.D. / Principal Investigator, University of Michigan
ClinicalTrials.gov Identifier: NCT00796094     History of Changes
Other Study ID Numbers: HUM 20943
Study First Received: November 21, 2008
Last Updated: November 24, 2009
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Soft Tissue Injuries
Wounds and Injuries

ClinicalTrials.gov processed this record on September 18, 2014