Clinical Trials Directory

Trials / Completed

CompletedNCT00673374

Correlation of Location of Abdominal Tenderness With Acute CT Abnormalities in Emergency Department Patients

Status
Completed
Phase
Study type
Observational
Enrollment
102 (actual)
Sponsor
Duke University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

To determine the correlation between the region of abdominal tenderness determined by the examining physician and the location of acute pathology diagnosed on abdominal CT. We hypothesize that the acute pathology diagnosed by CT will lie within the region marked on the abdominal wall by the examining physician prior to CT.

Conditions

Interventions

TypeNameDescription
DEVICEradio-opaque adhesive skin markersThe examining physician will place a radio-opaque skin marker (Beekley Corporation, Ortho-SPOTS® Order Code 187; 6mm spherical markers) at the point of maximal tenderness to direct abdominal palpation indicated by the patient. Additional markers will be placed at the cephalad and caudad limits of the region of tenderness, defined as the point at which the patient no longer complains of direct tenderness to palpation.

Timeline

Start date
2008-05-01
Primary completion
2009-01-01
Completion
2009-01-01
First posted
2008-05-07
Last updated
2014-02-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00673374. Inclusion in this directory is not an endorsement.