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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01769495
Other study ID # DE 6366-SP
Secondary ID
Status Completed
Phase N/A
First received January 14, 2013
Last updated April 13, 2017
Start date August 2013
Est. completion date September 2014

Study information

Verified date April 2015
Source University of North Carolina, Chapel Hill
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Our hypothesis is that a rapid follow up for elderly patients in a Geriatric Clinic discharged from the Emergency Department (ED) will have fewer unplanned return ED visits and fewer unplanned hospital admissions with no attendant increase in mortality.

Patients 75 years of age and older will be randomized following discharge from the ED into two groups. The first will receive standard post ED care. The second will receive an appointment to our Geriatric Clinic within 2-3 days for stabilization, further treatment and contact with the patient's primary physician to communicate the course of the patient's illness and to schedule subsequent follow-up with the patients regular medical provider.

There will be two primary outcomes: The first will be a composite of morality and/or return to the ED at 30 days, and the secondary primary outcome will be mortality. Economic data regarding resource utilization by patients will also be analyzed.


Recruitment information / eligibility

Status Completed
Enrollment 26
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers No
Gender All
Age group 75 Years and older
Eligibility Inclusion Criteria:

- All patients 75 years of age and older discharged from the ED

Exclusion Criteria:

- Younger than 75.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
2-3 day return appointment
2-3 appointment in geriatric clinic following ED discharge

Locations

Country Name City State
United States UNC Hospitals Chapel Hill North Carolina

Sponsors (3)

Lead Sponsor Collaborator
University of North Carolina, Chapel Hill The Duke Endowment, The William R. Kenan, Jr. Charitable Trust

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Medical Resource utilization 30 days and 180 days
Primary Mortality and readmissions to emergency department 30 and 180 days
Secondary Mortality Secondary outcome to measure all cause mortality for patients admitted to the study. 30 and 180 days
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