- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04390919
Prognostic Factors of Patients With ADHF
May 13, 2020 updated by: Dongying Zhang, Chongqing Medical University
Elevated Blood Monocyte Count Predicts 1 Year Poor Outcomes for Patients Admitted With Acute Decompensated Heart Failure
To explore the prognostic indicators for patients with ADHF
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
According to ESC Guidelines for the diagnosis of acute heart failure 2008, patients with ADHF were diagnosed, and their medical history, laboratory examination and treatment plan were retrospectively analyzed, and the patients were followed up for 1 year.
The 1-year outcomes of patients were analyzed to explore the prognostic indicators for patients with ADHF
Study Type
Observational
Enrollment (Actual)
362
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 to 94 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
ADHF patient diagnosed in the department of cardiovascular medicine in the first affiliated hospital of chongqing medical university
Description
Inclusion Criteria:
- Patients with ADHF diagnosed according to ESC Guidelines for the diagnosis of acute heart failure 2008
Exclusion Criteria:
- disorders of the hematopoietic system, history of cancer and/or previous treatment with chemotherapy, the infection caused by various pathogens, chronic inflammatory conditions, glucocorticoid therapy and/or histories of glucocorticoid use 3 months before the admission and acute myocardial infarction or coronary revascularization within the past 6 months. Also, patients who did not have a differential WBC count or who were lost to follow-up were excluded.
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 |
|---|---|
|
high group
high group: monocyte count≥0.445×10*9
cells/L
|
The monocyte count at admission was higher than 0.445×10*9 cells/L
|
|
low group
low group: monocyte count<0.445×10*9
cells/L;
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
all-cause death
Time Frame: 1 year
|
The primary end point was one-year all-cause death
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
HF-related rehospitalization
Time Frame: 1 year
|
the secondary end point was one-year HF-related rehospitalization.
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Actual)
August 2, 2011
Primary Completion (Actual)
February 16, 2015
Study Completion (Actual)
February 16, 2015
Study Registration Dates
First Submitted
May 4, 2020
First Submitted That Met QC Criteria
May 13, 2020
First Posted (Actual)
May 18, 2020
Study Record Updates
Last Update Posted (Actual)
May 18, 2020
Last Update Submitted That Met QC Criteria
May 13, 2020
Last Verified
May 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-05-04
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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