ClinicalTrials.Veeva

Menu

Heart Failure and Sleep Disordered Breathing

Y

Yihui Kong

Status

Enrolling

Conditions

Heart Failure

Study type

Observational

Funder types

Other

Identifiers

NCT05892172
2021020707

Details and patient eligibility

About

The purpose of this study is to analyze and summarize the characteristics of arrhythmia and heart rate variability of Chinese patients with three different types of heart failure combined with sleep disordered breathing based on the clinical data, to provide new diagnosis and treatment ideas for domestic patients, and then to improve the prognosis of patients betterly.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Age >18 years.
  2. The diagnosis of heart failure conforms to the criteria of the Chinese Guidelines for the Diagnosis and Treatment of Heart Failure .
  3. Echocardiography, dynamic electrocardiogram and polysomnography monitoring should be improved during the period of hospitalization.
  4. Patients with sleep apnea have not received standard treatment.

Exclusion criteria

  1. Patients undergoing cardiac surgery in the past 6 weeks.
  2. Patients with acute decompensated heart failure or heart failure requiring oxygen therapy.
  3. All patients with sleep apnea who receive standard treatment.
  4. Patients who use pacemakers or implantable cardioverter defibrillators.
  5. The patient did not complete the echocardiography, dynamic electrocardiogram, and polysomnography monitoring during hospitalization.

Trial design

300 participants in 3 patient groups

HFrEF group
Description:
HFrEF was defined as Left ventricular ejection fraction ≤40%
HFmrEF group
Description:
HFmrEF was defined as Left ventricular ejection fraction 41%\~49%
HFpEF group
Description:
HFpEF was defined as Left ventricular ejection fraction ≥50%

Trial contacts and locations

1

Loading...

Central trial contact

Yihui Kong, M.D.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems