Actively Recruiting

Age: 20Years - 100Years
All Genders
NCT05498584

Targeting LOXL2 and Cardiac Fibrosis for Post-acute Heart Failure Treatment- A Prospective Study

Led by Chang Gung Memorial Hospital · Updated on 2024-07-16

130

Participants Needed

1

Research Sites

209 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A previous study demonstrated that a multidisciplinary cardiac rehabilitation (CR) program was associated with reduced medium- to long-term all-cause mortality in a retrospective propensity score-matched study. The investigators will further investigate the predictors including LOXl2, cardiac MRI, and endothelial function that will benefit from a successful CR.

CONDITIONS

Official Title

Targeting LOXL2 and Cardiac Fibrosis for Post-acute Heart Failure Treatment- A Prospective Study

Who Can Participate

Age: 20Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients must give written informed consent before any assessment is performed.
  • Inpatients 20 years of age or older, male or female.
  • Diagnosis of heart failure New York Heart Association (NYHA) class II-IV with BNP 60;100 pg/mL or NT-proBNP 60;400 pg/mL (60;900 pg/mL if atrial fibrillation present).
  • Left ventricular ejection fraction 60;40% by echocardiography or other methods.
Not Eligible

You will not qualify if you...

  • Estimated survival time less than 6 months.
  • Long-term bedridden for more than 3 months.
  • Unable to tolerate exercise test due to muscular skeletal disorders.
  • Unable to cooperate with all functional studies.
  • Ventilator dependent.
  • Terminal heart status.
  • Family refuses participation in the project.
  • Primary severe valvular heart disease.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Chang Gung Memorial Hospital Heart Failure Center

Kaohsiung City, Taiwan, 83341

Actively Recruiting

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Research Team

H

Hsin-Yen Tsai

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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