- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04062500
Registry for Longitudinal Mortality and Therapy in Patients With Heart Failure (GREARTWAL)
Registry for Longitudinal Mortality and Therapy in Patients With Heart Failure (GREARTWAL Study)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Registry for Longitudinal mortality and therapy in patients with Heart Failure is a large, multicenter, prospective, open-label registry of the management of patients treated in the hospital for acute heart failure in China. The objective of this study is to investigate the clinical features and prognosis of patients with heart failure, and discover the characteristics of high-risk heart failure patients, and elucidate critical factors which predict the development and outcomes of symptomatic heart failure patients.
- To elucidate the clinical characteristics and prognostic risks of patients with heart failure.
- To study the characteristics of high-risk heart failure patients and predict the key factors for the development of symptomatic heart failure patients.
- To elucidate the compliance of patients with heart failure and the incidence of adverse drug effects.
- To investigate the effect of self-management on outcomes in patients with heart failure.
- To elucidate critical factors associated with the development and outcomes of heart failure.
- To investigate hospitalization expenses for heart failure.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Dachun Xu, PhD
- Phone Number: +86 18917684045
- Email: xdc77@tongji.edu.cn
Study Locations
-
-
Shanghai
-
Shanghai, Shanghai, China, 200072
- Recruiting
- Shanghai Tenth people's hospital, Tongji university
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- 1. 18 years and older. 2. Meet the diagnostic criteria of China 2018 or JACC/AHA 2017 or ESC 2016 heart failure guidelines.
3. Agree to be tested and sign an informed consent certificate.
Exclusion Criteria:
- 1. Age<18 years old. 2. Patients who refused to participate. 3. Patients may have a life expectancy of less than 1 years due to non- heart failure clinical conditions.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients with heart failure
patients treated in the hospital for acute heart failure in China
|
Mortality and Re-hospitalization of acute decompensated heart failure
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Mortality of acute decompensated heart failure
Time Frame: 10 years
|
In-hospital and Annual mortality
|
10 years
|
Re-hospitalization rate
Time Frame: 10 years
|
Re-hospitalization of acute decompensated heart failure
|
10 years
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Dachun Xu, PhD, Shanghai Tenthth People's Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GREARTWAL
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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