NCT01662843

Brief Summary

The B-RIPPED scan is a standardized ultrasound evaluation of pulmonary B-lines, Right ventricle size and strain, Inferior Vena Cava collapsibility, Pleural and Pericardial Effusion, Pneumothorax, Ejection Fraction, and lower extremity Deep Venous Thrombosis. Primary outcomes measured are the magnitude of change in differential diagnoses.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
104

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Oct 2011

Shorter than P25 for all trials

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

October 1, 2011

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

February 16, 2012

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2012

Completed
3 months until next milestone

First Posted

Study publicly available on registry

August 10, 2012

Completed
Last Updated

August 14, 2013

Status Verified

August 1, 2013

Enrollment Period

7 months

First QC Date

February 16, 2012

Last Update Submit

August 13, 2013

Conditions

Keywords

DyspneaUltrasonographyEmergenciesCritical Care

Outcome Measures

Primary Outcomes (1)

  • magnitude of change of differential diagnosis of the treating physician

    duration of ED course, which is expected to be an average of 3 hours

Secondary Outcomes (4)

  • time to complete the exam

    3 to 30 minutes during the ED course

  • time to disposition in control group compared to group receiving the BRIPPED scan

    duration of ED course, which is expected to be an average of 3 hours, with a range of 45 minutes to 6 hours

  • labs, consults, medications and other orders added or discontinued after the treating physician is informed of the BRIPPED scan results

    duration of the ED course, which is expected to be an average of 3 hours, with a range of 45 minutes to 6 hours

  • Recidivism rates among both cohorts, or evaluation of return to the ED within 30 days

    30 days after presentation to ED

Study Arms (2)

BRIPPED scan

Patients presenting with undifferentiated shortness of breath who receive the ultrasound scan in addition to standard of care

Control

Patients who only receive the standard of care for undifferentiated shortness of breath

Eligibility Criteria

Age18 Years - 89 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

A convenience sample of community subjects presenting to an Academic Hospital Emergency Department (volume approx 60,000 patients per year).

You may qualify if:

  • Subjects are included if they are between the ages of 18-89 and present to the Emergency Department with a chief complaint of shortness of breath or dyspnea.

You may not qualify if:

  • known history of asthma,
  • are 20 or more weeks pregnant, or
  • have had thoraco-abdominal trauma in the past 72 hours.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sentara Norfolk General Emergency Department

Norfolk, Virginia, 23507, United States

Location

Related Publications (1)

  • Stewart VM, Bjornsson HM, Clinton M, Byars DV. BRIPPED scan for evaluation of ED patients with shortness of breath. Am J Emerg Med. 2016 Mar;34(3):386-91. doi: 10.1016/j.ajem.2015.11.006. Epub 2015 Nov 5.

MeSH Terms

Conditions

DyspneaEmergencies

Condition Hierarchy (Ancestors)

Respiration DisordersRespiratory Tract DiseasesSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and SymptomsDisease AttributesPathologic Processes

Study Officials

  • Virginia M Stewart, MD

    Eastern Virginia Medical School

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 16, 2012

First Posted

August 10, 2012

Study Start

October 1, 2011

Primary Completion

May 1, 2012

Study Completion

May 1, 2012

Last Updated

August 14, 2013

Record last verified: 2013-08

Locations