NCT00724659

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
9

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2004

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2004

Completed
3.9 years until next milestone

First Submitted

Initial submission to the registry

July 28, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

July 29, 2008

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2010

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2010

Completed
Last Updated

May 3, 2012

Status Verified

May 1, 2012

Enrollment Period

5.9 years

First QC Date

July 28, 2008

Last Update Submit

May 1, 2012

Conditions

Joint Abnormalities

Keywords

ArthrogramContrastJointUltrasound

Outcome Measures

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.

    1 year

Study Arms (2)

Ultrasound Pre-Arthrogram

EXPERIMENTAL

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

Procedure: Ultrasound

Ultrasound Post-Arthrogram

EXPERIMENTAL

Ultrasound of the joint(s) after the clinically scheduled arthrogram of the same joint(s), performed while the body still has a contrast agent in it from the arthrogram. The contrast agent varies with different joint areas, but is usually iodine based (like Ultravist.)

Procedure: Ultrasound

Interventions

UltrasoundPROCEDURE

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

Ultrasound Pre-Arthrogram

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • clinically ordered arthrogram

You may not qualify if:

  • pregnant women
  • children under the age of 18

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Michigan Hospital

Ann Arbor, Michigan, 48109, United States

Location

MeSH Terms

Interventions

High-Energy Shock Waves

Intervention Hierarchy (Ancestors)

Ultrasonic WavesSoundRadiation, NonionizingRadiationPhysical Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

July 28, 2008

First Posted

July 29, 2008

Study Start

September 1, 2004

Primary Completion

August 1, 2010

Study Completion

November 1, 2010

Last Updated

May 3, 2012

Record last verified: 2012-05

Locations

US(1)