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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02812797
Other study ID # 2016-38-2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 2016
Est. completion date January 2020

Study information

Verified date March 2020
Source Chongqing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The purpose of this study is to determine whether expressions of adipokines can provide prognostic information concerning patients with chronic heart failure.


Recruitment information / eligibility

Status Completed
Enrollment 98
Est. completion date January 2020
Est. primary completion date August 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 80 Years
Eligibility Inclusion Criteria:

- Patients who are giving open chest surgical treatment with a history of chronic heart failure (NYHA II ~ IV) more than 6 months.

- Patients from whom informed consent has been properly obtained in writing prior to start of the trial.

Exclusion Criteria:

- Patients with concurrent infection or any documented inflammatory illness, such as arthritis or connective tissue diseases,or any other malignancy.

- Patients with a history of cardiomyopathy.

- Patients with Chronic arrhythmia.

- Pregnant women

- Severe hepatic dysfunction or End-stage renal failure.

- Uncontrolled hypertension.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China The First Affiliated Hospital of Chongqing Medical University Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Chongqing Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary All-cause mortality Change from Baseline at 3, 6 and 12 months
Secondary New York Heart Association (NYHA) Classification Week:4
Secondary re-hospitalization Heart failure with re-hospitalization is documented by at least one of the following: worse exercise tolerance and respiratory distress with NYHA class III or IV symptoms, presence of pulmonary rales, or chest radiography showing pulmonary congestion, which needs an augmented decongestive regimen with oral or intravenous medications during an in-hospital stay. Change from Baseline at 3, 6 and 12 months
Secondary plasma brain natriuretic peptide (BNP) concentration Week:4
Secondary Cardiovascular death Change from Baseline at 3, 6 and 12 months
Secondary Cardiac transplantation Change from Baseline at 3, 6 and 12 months
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