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OpenTrials
Completed

NCT Number: NCT00724659

Pre and Post Arthrogram Ultrasound Images of Joints

The purpose of this study is to determine the usefulness of contrast in ultrasonography of the joints.

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Key information

Conditions

Joint Abnormalities

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Michigan Hospital

Ann Arbor, Michigan, 48109, United States

About this study

To determine if using intra-articular contrast (contrast injected into a joint) will provide clearer, more precise ultrasound images of the joints then an ultrasound done without the use of a contrast agent.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • clinically ordered arthrogram

Exclusion criteria

  • pregnant women
  • children under the age of 18

Treatment and study plan

Ultrasound

Procedure

Ultrasound of the joint(s) before the clinically scheduled arthrogram of the same joint(s)

Primary outcomes

  1. To add to the general knowledge of the researchers and to possibly benefit future patients in the diagnosis and treatment of joint abnormalities.

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

University of Michigan

Other

Registry information

Official study title

An Evaluation of Pre and Post Arthrogram Ultrasound Images of Joints: Does Arthrography Have a Role in Ultrasonography?

Important dates

Study start
2004
Primary completion
2010
Study completion
2010
First posted
Jul 29, 2008
Registry last updated
May 3, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.