bisoprolol has been researched along with Death, Sudden, Cardiac in 14 studies
Bisoprolol: A cardioselective beta-1 adrenergic blocker. It is effective in the management of HYPERTENSION and ANGINA PECTORIS.
Death, Sudden, Cardiac: Unexpected rapid natural death due to cardiovascular collapse within one hour of initial symptoms. It is usually caused by the worsening of existing heart diseases. The sudden onset of symptoms, such as CHEST PAIN and CARDIAC ARRHYTHMIAS, particularly VENTRICULAR TACHYCARDIA, can lead to the loss of consciousness and cardiac arrest followed by biological death. (from Braunwald's Heart Disease: A Textbook of Cardiovascular Medicine, 7th ed., 2005)
Excerpt | Relevance | Reference |
---|---|---|
"Whether all patients with congestive heart failure (CHF) need to reach the target dose of beta-blocker to obtain a benefit in terms of survival remains uncertain." | 6.71 | Bisoprolol dose-response relationship in patients with congestive heart failure: a subgroup analysis in the cardiac insufficiency bisoprolol study(CIBIS II). ( Funck-Brentano, C; Jaillon, P; Lechat, P; Mary-Krause, M; Simon, T, 2003) |
"Baroreflex sensitivity was assessed in 287 patients with history of myocardial infarction and left ventricular ejection fraction < or =40% by phenylephrine test and was found to be depressed (4." | 3.72 | [Correction of baroreflex sensitivity impairment and efficacy of prevention of sudden arrhythmic death in patients with postinfarction left ventricular dysfunction]. ( Bozhko, AA; Kanopskiĭ, SG; Staritskiĭ, AG, 2004) |
"The occurrence of sudden cardiac death (SCD) in patients with silent ischemia after myocardial infarction (MI) and the factors facilitating SCD are unknown." | 2.74 | Sudden cardiac death in patients with silent myocardial ischemia after myocardial infarction (from the Swiss Interventional Study on Silent Ischemia Type II [SWISSI II]). ( Abbate, A; Erne, P; Jamshidi, P; Kobza, R; Pfisterer, M; Schoenenberger, AW; Stuck, AE; Zuber, M, 2009) |
"Whether all patients with congestive heart failure (CHF) need to reach the target dose of beta-blocker to obtain a benefit in terms of survival remains uncertain." | 2.71 | Bisoprolol dose-response relationship in patients with congestive heart failure: a subgroup analysis in the cardiac insufficiency bisoprolol study(CIBIS II). ( Funck-Brentano, C; Jaillon, P; Lechat, P; Mary-Krause, M; Simon, T, 2003) |
"The heart failure is one of the pathologies with major social and economic impact in the western world." | 2.44 | [Chronic heart failure and sudden death: the message of CIBIS-III]. ( Dequarti, MC; Poggio, L; Vanoli, E, 2007) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (21.43) | 18.2507 |
2000's | 8 (57.14) | 29.6817 |
2010's | 1 (7.14) | 24.3611 |
2020's | 2 (14.29) | 2.80 |
Authors | Studies |
---|---|
Sánez Tähtisalo, H | 1 |
Hiltunen, TP | 1 |
Kenttä, T | 1 |
Junttila, J | 1 |
Oikarinen, L | 1 |
Virolainen, J | 1 |
Kontula, KK | 1 |
Porthan, K | 1 |
Sirico, G | 1 |
Montisci, A | 1 |
Secchi, F | 1 |
Mantica, M | 1 |
Schoenenberger, AW | 2 |
Kobza, R | 1 |
Jamshidi, P | 1 |
Zuber, M | 2 |
Abbate, A | 1 |
Stuck, AE | 1 |
Pfisterer, M | 2 |
Erne, P | 2 |
Krum, H | 1 |
van Veldhuisen, DJ | 1 |
Funck-Brentano, C | 2 |
Vanoli, E | 2 |
Silke, B | 1 |
Erdmann, E | 1 |
Follath, F | 1 |
Ponikowski, P | 1 |
Goulder, M | 1 |
Meyer, W | 1 |
Lechat, P | 2 |
Willenheimer, R | 1 |
Simon, T | 1 |
Mary-Krause, M | 1 |
Jaillon, P | 1 |
Kanopskiĭ, SG | 1 |
Staritskiĭ, AG | 1 |
Bozhko, AA | 1 |
Kowey, PR | 1 |
Burckhardt, D | 1 |
Kiowski, W | 1 |
Dubach, P | 1 |
Resink, T | 1 |
Dequarti, MC | 1 |
Poggio, L | 1 |
Drummond, GA | 1 |
Squire, IB | 1 |
Kendall, MJ | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Long Term Study on the Possible Beneficial Effects of Catheterised Renal Denervation in Patients With Heart Failure and Left Ventricular Systolic Dysfunction Who Are Already on Standard Medical Therapy.[NCT01870310] | 50 participants (Anticipated) | Interventional | 2012-06-30 | Recruiting | |||
Bisoprolol Plasma Residual Concentrations for the Optimization of Drug Management in Heart Failure With Mild to Reduced Ejection Fraction[NCT03644446] | 81 participants (Anticipated) | Observational [Patient Registry] | 2017-11-02 | Recruiting | |||
A Multicenter,Randomized, Double Blind, Double Dummy, Parallel Group Study to Compare Effects of Coreg CR and Coreg IR on Left Ventricular End Systolic Volume Index in Subjects With Stable Chronic Heart Failure[NCT00323037] | Phase 3 | 318 participants (Actual) | Interventional | 2006-03-31 | Completed | ||
Collaborative Systematic Overview of Randomised Controlled Trials of Beta-Blockers in the Treatment of Heart Failure[NCT00832442] | 18,240 participants (Anticipated) | Observational | 2008-08-31 | Enrolling by invitation | |||
The PACE-MI Registry Study - Outcomes of Beta-blocker Therapy After Myocardial Infarction (OBTAIN)[NCT00430612] | 7,057 participants (Actual) | Observational [Patient Registry] | 2009-05-31 | Completed | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | -0.88 |
Carvedilol Controlled Release | -0.86 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | 24.00 |
Carvedilol Controlled Release | 53.37 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | -0.20 |
Carvedilol Controlled Release | -0.45 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | -0.33 |
Carvedilol Controlled Release | -0.36 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | -0.76 |
Carvedilol Controlled Release | -0.83 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | .08 |
Carvedilol Controlled Release | .05 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | .08 |
Carvedilol Controlled Release | .08 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | -36.61 |
Carvedilol Controlled Release | -42.22 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | -18.29 |
Carvedilol Controlled Release | -20.57 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | -36.61 |
Carvedilol Controlled Release | -43.00 |
Maintenance Visit 3 minus Baseline. Maintenance Visit 3 occurred 24 weeks after entry into the maintenance period. The maintenance period started after completion of a titration period of variable duration. (NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | mL/m^2 (Mean) |
---|---|
Coreg Immediate Release | -18.36 |
Coreg Controlled Release | -20.81 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | 9.5 |
Carvedilol Controlled Release | -9.29 |
(NCT00323037)
Timeframe: 24 weeks after entry into the maintenance period
Intervention | percentage of change (Mean) |
---|---|
Carvedilol Immediate Release | .07 |
Carvedilol Controlled Release | .05 |
SAEs experienced (NCT00323037)
Timeframe: 24 weeks after entry into the maintenance phase (after unblinding)
Intervention | number of SAEs (Number) |
---|---|
Carvedilol Immediate Release | 40 |
Carvedilol Controlled Release | 35 |
(NCT00323037)
Timeframe: Up to 32 weeks (titration and maintenance phases)
Intervention | subjects in each treatment group (Number) | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Study Entry (10mg Coreg CR, 3.125mg Coreg IR) | Maintenance Entry (10mg Coreg CR, 3.125mg Coreg IR) | End of Study (10mg Coreg CR, 3.125mg Coreg IR) | Study Entry (20mg Coreg CR, 6.25mg Coreg IR) | Maintenance Entry (20mg Coreg CR, 6.25mg Coreg IR) | End of Study (20mg Coreg CR, 6.25mg Coreg IR) | Study Entry (40mg Coreg CR, 12.5mg Coreg IR) | Maintenance Entry (40mg Coreg CR, 12.5mg Coreg IR) | End of Study (40mg Coreg CR, 12.5mg Coreg IR) | Study Entry (80mg Coreg CR, 25mg Coreg IR) | Maintenance Entry (80mg Coreg CR, 25mg Coreg IR) | End of Study (80mg Coreg CR, 25mg Coreg IR) | |
Carvedilol Controlled Release | 83 | 0 | 4 | 39 | 9 | 16 | 27 | 16 | 22 | 4 | 114 | 111 |
Carvedilol Immediate Release | 79 | 0 | 7 | 61 | 13 | 16 | 21 | 12 | 21 | 4 | 116 | 121 |
(NCT00323037)
Timeframe: Up to 32 weeks (titration and maintenance phases)
Intervention | participants in each treatment group (Number) | ||
---|---|---|---|
Hospitalization for Heart Failure | Hospitalization Due to Any Cause | Hospitalization or Death | |
Carvedilol Controlled Release | 6 | 29 | 29 |
Carvedilol Immediate Release | 6 | 31 | 32 |
2 reviews available for bisoprolol and Death, Sudden, Cardiac
Article | Year |
---|---|
A review of carvedilol arrhythmia data in clinical trials.
Topics: Adrenergic beta-Antagonists; Amiodarone; Anti-Arrhythmia Agents; Atrial Fibrillation; Bisoprolol; Ca | 2005 |
[Chronic heart failure and sudden death: the message of CIBIS-III].
Topics: Adrenergic beta-Antagonists; Aged; Angiotensin-Converting Enzyme Inhibitors; Antihypertensive Agents | 2007 |
5 trials available for bisoprolol and Death, Sudden, Cardiac
Article | Year |
---|---|
Sudden cardiac death in patients with silent myocardial ischemia after myocardial infarction (from the Swiss Interventional Study on Silent Ischemia Type II [SWISSI II]).
Topics: Adrenergic beta-Antagonists; Adult; Aged; Amlodipine; Angioplasty, Balloon, Coronary; Antihypertensi | 2009 |
Effect on mode of death of heart failure treatment started with bisoprolol followed by Enalapril, compared to the opposite order: results of the randomized CIBIS III trial.
Topics: Adrenergic beta-Antagonists; Aged; Angiotensin-Converting Enzyme Inhibitors; Bisoprolol; Chronic Dis | 2011 |
Bisoprolol dose-response relationship in patients with congestive heart failure: a subgroup analysis in the cardiac insufficiency bisoprolol study(CIBIS II).
Topics: Adrenergic beta-Antagonists; Bisoprolol; Death, Sudden, Cardiac; Dose-Response Relationship, Drug; D | 2003 |
Effects of anti-ischaemic drug therapy in silent myocardial ischaemia type I: the Swiss Interventional Study on Silent Ischaemia type I (SWISSI I): a randomized, controlled pilot study.
Topics: Acute Coronary Syndrome; Adrenergic beta-Antagonists; Adult; Aged; Amlodipine; Bisoprolol; Death, Su | 2007 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
The Cardiac Insufficiency Bisoprolol Study II (CIBIS-II): a randomised trial.
Topics: Adrenergic beta-Antagonists; Adult; Aged; Aged, 80 and over; Bisoprolol; Death, Sudden, Cardiac; Dou | 1999 |
7 other studies available for bisoprolol and Death, Sudden, Cardiac
Article | Year |
---|---|
Effect of four classes of antihypertensive drugs on cardiac repolarization heterogeneity: A double-blind rotational study.
Topics: Adrenergic beta-Antagonists; Angiotensin Receptor Antagonists; Antihypertensive Agents; Bisoprolol; | 2020 |
Myotonic dystrophy type 1 and high ventricular vulnerability at the electrophysiological evaluation: ICD yes or not?
Topics: Adrenergic beta-1 Receptor Antagonists; Adult; Bisoprolol; Clinical Decision-Making; Death, Sudden, | 2020 |
[Longevity promoting beta blocker. Soon in 1st place in heart failure?].
Topics: Adrenergic beta-Antagonists; Angiotensin-Converting Enzyme Inhibitors; Bisoprolol; Cause of Death; C | 2003 |
[Correction of baroreflex sensitivity impairment and efficacy of prevention of sudden arrhythmic death in patients with postinfarction left ventricular dysfunction].
Topics: Adrenergic beta-Antagonists; Adult; Aged; Amiodarone; Angiotensin-Converting Enzyme Inhibitors; Anti | 2004 |
[Beginning therapy of heart failure with beta blockers. Do these patients survive longer?].
Topics: Adrenergic beta-Antagonists; Angiotensin-Converting Enzyme Inhibitors; Bisoprolol; Death, Sudden, Ca | 2005 |
The Cardiac Insufficiency Bisoprolol Study II.
Topics: Adrenergic beta-Antagonists; Bisoprolol; Death, Sudden, Cardiac; Heart Failure; Humans | 1999 |
Possible mechanisms of action in the positive effect of beta blockers in heart failure.
Topics: Adrenergic beta-Antagonists; Bisoprolol; Death, Sudden, Cardiac; Heart Failure; Humans; Myocardial I | 1999 |