Heart Valve Disease Clinical Trial
Official title:
Effect of Heart Valve Replacement on Cheyne-Stokes Respiration in Patients With Rheumatic Heart Disease
Sleep disordered breathing, especially central sleep apnea, is common in patients with chronic heart failure. Heart valve replacement could have some effect on central sleep apnea. The aim of the study is to investigate effect of heart valve replacement on Cheyne-Stokes respiration in patients with rheumatic heart disease.
Sleep apnea, especially central sleep apnea, has a high prevalence in patients with chronic
heart failure. Although sleep disordered breathing (SDB) have been described in patients with
heart disease, the prevalence is not known because: ①There are various forms of SDBs,
including obstructive sleep apnea(OSA), central sleep apnea (CSA), and mixed forms of sleep
apnea syndromes that have variable prevalence; ②Patients suffering from rheumatic valve
disease usually have varying degrees of heart failure, and this variability affects estimates
of prevalence; ③There are no international patient registries and SDB is underdiagnosed in
many parts of the world.
The previous studies are most focusing on nonvalvular disease. We ①investigate the prevalence
and the risk factors of Cheyne-Stokes respiration in patients with heart valve diseases,
②compare the changes of parameters of Cheyne-Stokes Respiration and heart function (like
apnea hypopnea index, pulse oxygen saturation, blood pressure, echocardiogram,
electrocardiogram, 6-minute walk test) before heart valve replacement and 3, 6, and 12 months
after the surgery.
With nocturnal polysomnography (PSG) examination 30 patients typical CSR are going to be
screened out from 300 patients with heart valve disease and waiting for cardiac surgery. The
Comparison of 30 patients undergoing heart valve replacement will be performed before and 3,
6, and 12 months following heart valve replacement. We shall analyze the changes of CSR
before and after valve replacement as well as the correlation among cardiac function and PSG
parameters.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06027788 -
CTSN Embolic Protection Trial
|
N/A | |
Completed |
NCT02527629 -
Aortic Replacement Using Individualised Regenerative Allografts - ARISE (the "Surveillance")
|
||
Completed |
NCT01178710 -
Effect of Simvastatin on Cardiac Function
|
N/A | |
Completed |
NCT00581399 -
A Randomized Multicenter Clinical Study On the High Vacuum Body Cavity Drainage System Following Open Heart Surgery
|
Phase 2 | |
Withdrawn |
NCT00187304 -
ACTION - Anticoagulation Treatment Influence on Post-operative Patients
|
Phase 4 | |
Terminated |
NCT00700947 -
Using Beta Blockers to Treat Mitral Regurgitation
|
Phase 1 | |
Recruiting |
NCT02650388 -
Frailty and Cognitive Function Assessment of TAVI Patients
|
Phase 4 | |
Recruiting |
NCT02574650 -
Early Feasibility of the Mitralign Percutaneous Tricuspid Valve Annuloplasty System (PTVAS) Also Known as TriAlign™.
|
N/A | |
Completed |
NCT01996657 -
D-dimer and Oral Anticoagulation Therapy in Patients With Mechanical Valve Replacement
|
N/A | |
Terminated |
NCT00598936 -
A Prospective Study With a New Device for the Monitoring of Cerebral Oxygenation on Cardiac Surgery Patients
|
Phase 1 | |
Terminated |
NCT01812174 -
On-X Heart Valve - 17mm Aortic and 23mm Mitral
|
N/A | |
Recruiting |
NCT03225612 -
Safety and Performance of the Trialign Percutaneous Tricuspid Valve Annuloplasty System (PTVAS)
|
N/A | |
Completed |
NCT01384643 -
Effect of Propofol on Renal Injury in Patients Undergoing Valvular Heart Surgery
|
Phase 4 | |
Completed |
NCT01558765 -
CopenHeartVR - Integrated Rehabilitation of Patients After Heart Valve Surgery
|
Phase 2 | |
Active, not recruiting |
NCT00291525 -
Randomized On-X Anticoagulation Trial
|
N/A | |
Completed |
NCT02867930 -
Comparative Effects of Dexmedetomidine and Ketofol for Sedation in Patients Undergoing Trans-esophageal Echocardiography
|
Phase 4 | |
Recruiting |
NCT02478008 -
A Clinical Study of the CardiAQ™ TMVI System (Transapical DS)
|
N/A | |
Completed |
NCT02790008 -
Magnetic Resonance Imaging and Fibrosis
|
||
Completed |
NCT02587039 -
An Intervention to Reduce Delirium After Cardiac Surgery
|
N/A | |
Recruiting |
NCT01855737 -
The Study of Warfarin Maintenance Dose in Chinese Patients
|
Phase 4 |