- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01373775
Risk Factors of the Revisit of the Adult Heart Failure Patients in Emergency Department Siriraj Hospital
June 14, 2011 updated by: Mahidol University
Risk Factors of the Revisit of the Adult Heart Failure Patients in Emergency Department in Siriraj Hospital: The One Year Period.
To identify the risk factors of the revisit of the adult HF patients in emergency department.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Because heart failure (HF) is the leading cause of hospitalization and readmission in many hospitals worldwide.
Identifying the risk factors of these HF patients in emergency department is the important reason for the proper management of the HF patients in the future. And can reduce number of hospitalization and readmission in our hospital.
Study Type
Observational
Enrollment (Actual)
533
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Bangkok, Thailand, 10700
- Emergency department, Siriraj hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Medical records of 533 patients,who visited the emergency department with the diagnosis of HF (ICD-10 I500, I501 and I509) in the period from 1st Jan 2008 to 31st Dec 2008, were reviewed.
Description
Inclusion Criteria:
- Patients age from 18 years old
- Patients who were diagnosed HF by the Framingham's criteria10
- Patients who were discharged home from emergency department
Exclusion Criteria:
- Patients age less than 18 years old
- Patients who not met Framingham's criteria, needed hospital admission, were referred to other hospital, and death
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Revisit
HF patients who revisit the emergency department before the next appointment date.
|
Reviewing chart and identifying risk factors
|
Non-revisit
HF patients who follow up on the appointment date.
|
Reviewing chart and identifying risk factors
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of HF patients who were revisited emergency department before the appointment date.
Time Frame: 1 year
|
All HF-peatient charts were reviewed and divided in revisit group and non revisit group.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Characteristics of the patients in revisit group
Time Frame: 1 year
|
The Characteristics of the patients in both groups such as underlying diseases, ejection fraction, and time for treating in emergency department.
The results were compared to find the relation between both groups.
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Phuriphong Songarj, MD, Department of Anesthesiology
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2009
Primary Completion (Actual)
September 1, 2009
Study Completion (Actual)
February 1, 2010
Study Registration Dates
First Submitted
June 9, 2011
First Submitted That Met QC Criteria
June 14, 2011
First Posted (Estimate)
June 15, 2011
Study Record Updates
Last Update Posted (Estimate)
June 15, 2011
Last Update Submitted That Met QC Criteria
June 14, 2011
Last Verified
June 1, 2011
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 740/2551(EC1)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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