Important Note: Redirection of Services to ChiCTR
We would like to inform you that the Clinical Trial Registry page will discontinue the function of updating trial information directly on this platform. However, you will still be able to view the existing registration details. For any updates to trial information, you can use the China Clinical Trial Registry (ChiCTR) directly at https://www.chictr.org.cn. This change will be fully implemented by 2024-Aug-05. Thank you for your attention.
CUHK_CCT00250
2010-07-06
Retrospective
Nil
RGC funding for the study
RGC funding
Nil
Cheuk Man Yu
Rm. 12A28, 12/F, Main Building, PWH
2632 1752
cmyu@cuhk.edu.hk / poonsp@cuhk.edu.hk
Nil
Cheuk Man Yu
Rm.12A28, 12/F, main building, PWH
2632 1752
cmyu@cuhk.edu.hk / poonsp@cuhk.edu.hk
Nil
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
Nil
Hong Kong
Yes
2007-03-13
Heart failure (HF)
Procedure
Echocardiography assesses LV asynchrony in both systole and diastole of Acute Heart Failure Decompensation in Patients.
4 years
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 (contraction) and diastole (relaxation), which include the tissue Doppler imaging (TDI) and real-time 3-dimensional echocardiography (3DE). 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 prevalence and severity of cardiac systolic and diastolic asynchrony. 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, patients will enter into the prospective study and will be followed up at 1, 3 and 6 months, and the changes of systolic and diastolic asynchrony will be examined by echocardiography and compared between the 2 HF groups. 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 patients with recent acute HF decompensation, and whether it will contribute to exercise-induced mitral regurgitation.
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
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
Patient > 18 years of age
Patient > 18 years of age
Both Male and Female
Observational
Non-randomized
Active
Open label
Parallel
2008-02-15
150patiens
Unknown
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
Nil
2014-01-29
ChiCTR-OCC-10001033
2010-10-15
|
|
|
|
---|---|---|---|
No documents yet. |