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Impact of Left Ventricular Asynchrony in the Development of Acute Heart Failure Decompensation in Patients with Systolic Dysfunction

Impact of Left Ventricular Asynchrony in the Development of Acute Heart Failure Decompensation in Patients with Systolic Dysfunction

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OCC-10001033
Enrollment
Unknown
Registered
2010-07-06
Start date
2008-02-15
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart failure (HF)

Interventions

Two groups:Echocardiography assesses LV asynchrony in both systole and diastole of Acute Heart Failure Decompensation in Patients for 4 years
2 groups:The study is a prospective, case-control design. It will employ advanced and sensitive echocardiographic technologies (ultrasound of the heart) to examine LV asynchrony in both systole (contr
1:In the cross-sectional study, 75 patients hospitalized for acute HF decompensation will be compared with another 75 patients with chronic stable HF to examine whether there are difference in the pre
1:This will be performed by using a number of validated parameters of asynchrony based on TDI and 3DE, and 75 normal controls will be selected to provide the reference normal cutoff values. Then, pati
1: Lastly, these patients will undergo exercise stress echocardiography at or before 1-month follow up to test the hypothesis whether dynamic LV asynchrony is a common condition in the group of HF pat

Sponsors

RGC funding
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1) Two groups of patients will be enrolled: (1) Patients who are admitted to acute medical ward for a diagnosis of acute HF (both first time presentation of HF or acute deterioration of chronic HF); (2) Patients with chronic stable HF who had no evidence of decompensation over the past 6 months; and 2) evidence of left ventricular (LV) systolic dysfunction with ejection fraction <50%; and, 3) normal QRS duration of <120ms.

Exclusion criteria

Exclusion criteria: 1) HF with ejection fraction >50%; 2) HF with wide QRS complex of >120ms; 3) Patients with fluid overload due to other conditions, such as renal failure or non-cardiogenic pulmonary oedema; 4) Patients with HF due to cardiac arrhythmia, thyrotoxicosis and other causes of high output HF; 5) Patients with atrial fibrillation that will preclude accurate analysis of systolic asynchrony, in particular 3DE; 6) Patients with poor image quality that preclude echocardiographic analysis; 7) Patients with disease with expected life expectancy 6 months, such as malignancies; 8) Patients who refuse to participate the study.

Design outcomes

Primary

MeasureTime frame
1) LV ejection fraction; 2) LV end-systolic volume; 3) Asynchrony Index by TDI (Ts-SD); 4) Asynchrony Index by 3DE (Tmrv-16); 5) Difference in prevalence of dyssynchrony between 2 HF gps; 6) Change in prevalence of dyssynchrony within acute HF gp; 7) 6 minutes walk; 8) SF-36? Health Survey Questionnaire; 9) Neurohormonal levels;

Contacts

Public ContactCheuk Man Yu
poonsps@yahoo.com.hk+852 2632 1752

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026