NCT00146354

CompletedPhase 3

The Effects of a Results Management System on Physician Awar...

Brigham and Women's Hospital Source

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Other study identifiers

Sponsor study identifier

2003P000551

Study Type

interventional

Reported enrollment (type unavailable)

N/A

Locations

1 country

Sites

2

Timeline

Study Start

Not reported

Date not reported

Primary Completion

Not reported

Date not reported

Study Completion

Not reported

Date not reported

Brief Summary

This project aims to define the problem of results that return after patient discharge and to study the implementation of an Electronic Medical Record (EMR)-based system for tracking these results.

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Reported enrollment (type unavailable): Not reported
Study completion date: Not reported
Date not reported
Listed locations: 1 countries · 2 sites

Trial Relationships

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Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

First Submitted
September 2, 2005
Actual (reported)
First Posted
September 7, 2005
Actual (reported)

Last Updated: March 2, 2007
Status Verified: August 2005
Last Update Submitted: March 1, 2007

Conditions

Healthy Medical Record Systems, Computerized

Keywords

Electronic Medical RecordElectronic Results TrackingPatient SafetyPost-Discharge Test Results

Interventions

Hospitalists Results ManagerBehavioral

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

Eligibility Criteria

Age18 Years+

Sexall

Healthy VolunteersYes

Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

Admitted under enrolled study Attendings at the two study locations
Patient had test result finalized after discharge and prior to subsequent admission

You may not qualify if:

Sponsors & Collaborators

Harvard Risk Management Foundation
Othercollaborator
Brigham and Women's Hospital
Otherlead

Study Sites (2)

Massachusetts General Hospital

Boston, Massachusetts, 02114, United States

Brigham and Women's Hospital

Boston, Massachusetts, 02120, United States

Study Officials

Tejal K Gandhi, MD, MPH
Brigham and Women's Hospital
PRINCIPAL INVESTIGATOR

Study Design

Study Type: interventional
Phase: phase 3
Allocation: NON RANDOMIZED
Masking: SINGLE
Purpose: ECT
Intervention Model: PARALLEL
Sponsor Type: OTHER

Study Record Dates

First Submitted

September 2, 2005

First Posted

September 7, 2005

Last Updated

March 2, 2007

Record last verified: 2005-08

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.