carvedilol has been researched along with Dyslipidemias in 2 studies
Dyslipidemias: Abnormalities in the serum levels of LIPIDS, including overproduction or deficiency. Abnormal serum lipid profiles may include high total CHOLESTEROL, high TRIGLYCERIDES, low HIGH DENSITY LIPOPROTEIN CHOLESTEROL, and elevated LOW DENSITY LIPOPROTEIN CHOLESTEROL.
Excerpt | Relevance | Reference |
---|---|---|
"We aimed to investigate the acute and chronic effects of carvedilol on insulin resistance in high-fructose, high-fat diet (HFrHFD) - fed mice and the implication of the β-arrestin2 pathway." | 4.12 | Acute and chronic metabolic effects of carvedilol in high-fructose, high-fat diet-fed mice: implication of β-arrestin2 pathway. ( Ahmed, HMS; Ibrahim, IAAE; Ibrahim, WS; Mahmoud, AAA; Mahmoud, MF; Mohamed, SG; Rezk, AM, 2022) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (50.00) | 2.80 |
Authors | Studies |
---|---|
Ahmed, HMS | 1 |
Mohamed, SG | 1 |
Ibrahim, WS | 1 |
Rezk, AM | 1 |
Mahmoud, AAA | 1 |
Mahmoud, MF | 1 |
Ibrahim, IAAE | 1 |
Bakris, GL | 1 |
Tarka, EA | 1 |
Waterhouse, B | 1 |
Goulding, MR | 1 |
Madan, A | 1 |
Anderson, KM | 1 |
St John Sutton, M | 1 |
Miller, AB | 1 |
Reichek, N | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Randomized, Double-Blind, Multi-Center Study Comparing the Effects of Carvedilol Modified Release Formulation (COREG MR) and Atenolol in Combination With and Compared to an Angiotensin Converting Enzyme Inhibitor (Lisinopril) on Left Ventricular Mass Re[NCT00108082] | Phase 3 | 287 participants (Actual) | Interventional | 2005-01-31 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
LV Mass was measured by MRI at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | grams (g) (Mean) |
---|---|
Carvedilol CR | -13.74 |
Atenolol | -14.17 |
Lisinopril | -17.17 |
LVMI was measured by echogradiography at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | grams per meters squared (g/m^2) (Mean) |
---|---|
Carvedilol CR | -20.35 |
Atenolol | -20.06 |
Lisinopril | -18.48 |
LVMI was measured by MRI at Baseline and after 12 months of treatment/Month 12. A reduction in left ventricular mass, calculated as LVMI, of 5 g/m^2 was assumed to be clinically meaningful. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the Last Observation Carried Forward [LOCF] analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | grams per meters squared (g/m^2) (Mean) |
---|---|
Carvedilol CR | -6.34 |
Atenolol | -6.67 |
Lisinopril | -7.94 |
LVMIH was measured by echogradiography at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was available)
Intervention | g/m raised to 2.7 (g/(m^2.7)) (Mean) |
---|---|
Carvedilol CR | -11.78 |
Atenolol | -12.51 |
Lisinopril | -11.61 |
LVMIH was measured by MRI at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. LV mass depends on body size. One method of determining whether an individual has LV hypertrophy relates LV mass to height raised to a power of 2.7. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | g/m raised to 2.7 (g/(m^2.7)) (Mean) |
---|---|
Carvedilol CR | -3.19 |
Atenolol | -3.37 |
Lisinopril | -3.98 |
LV Mass was measured by echocardiography at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | grams (Mean) |
---|---|
Carvedilol CR | -45.76 |
Atenolol | -40.56 |
Lisinopril | -38.58 |
Urinary ACR (micrograms per milligram) was determined at Baseline and after 12 months of treatment/Month 12. Percentage change from Baseline was based on log transformed data and was calculated as 100 x (exponent (exponent (mean change on log scale) - 1. [Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value.] (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF was used)
Intervention | percentage of change (Geometric Mean) |
---|---|
Carvedilol CR | -27.1 |
Atenolol | -20.1 |
Lisinopril | -21.5 |
BNP concentration (picagram per milliter) was measured at Baseline and after 12 months of treatment/Month 12. Percentage change from Baseline was based on log transformed data and was calculated as 100 x (exponent (mean change on log scale) -1) [Change is the Month 12 value (or value after 12 months of treatment) minus the Baseline value]. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF was used
Intervention | percentage of change (Geometric Mean) |
---|---|
Carvedilol CR | 51.7 |
Atenolol | 48.3 |
Lisinopril | -39.1 |
CRP concentration (milligrams per deciliter) was measured at Baseline and after 12 months of treatment/Month 12. Percentage change from Baseline was based on log transformed data and calculated as 100 x (exponent (mean change on log scale) - 1). [Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value.] (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF was used)
Intervention | percentage of change (Geometric Mean) |
---|---|
Carvedilol CR | -10.63 |
Atenolol | -3.22 |
Lisinopril | 2.70 |
LV filling parameters, LV E-Volume and LV A-Volume, were measured by MRI at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. These filling parameters represent the volumes of blood filling the ventricle during the passive filling phase (E-volume) and the active filling phase caused by atrial contraction (A-volume). (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | milliliters (mL) (Mean) | |
---|---|---|
LV E-volume | LV A-volume | |
Atenolol | 6.763 | -0.565 |
Carvedilol CR | 0.364 | -0.513 |
Lisinopril | -3.406 | 1.088 |
LV End Systolic and Diastolic Volumes and Ejection Fraction were measured by echocardiography at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | milliliters (mL) (Mean) | ||
---|---|---|---|
LV End Systolic Volume | LV End Diastolic Volume | LV Ejection Fraction | |
Atenolol | -4.74 | -3.64 | 2.33 |
Carvedilol CR | -3.38 | -3.07 | 1.03 |
Lisinopril | -5.34 | -9.37 | 0.63 |
LV End Systolic and Diastolic Volumes and Ejection Fraction were measured by MRI at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. The ejection fraction is the fraction of the blood volume available at the end of diastole that is pumped out of the ventricules during systole. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | milliliters (mL) (Mean) | ||
---|---|---|---|
LV End Systolic Volume | LV End Diastolic Volume | LV Ejection Fraction | |
Atenolol | -4.29 | -2.45 | 2.16 |
Carvedilol CR | -1.44 | -2.86 | 0.08 |
Lisinopril | -3.04 | -7.45 | -0.01 |
Systolic and Diastolic BP were measured at Baseline and after 12 months of treatment/Month 12. Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value. (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF analysis, which includes data collected on or after Month 9 of treatment to Month 12 of treatment, was used)
Intervention | mmHg (millimeters of mercury) (Mean) | |
---|---|---|
Systolic blood pressure | Diastolic blood pressure | |
Atenolol | -21.12 | -14.05 |
Carvedilol CR | -21.32 | -12.77 |
Lisinopril | -22.53 | -11.13 |
Plasma lipid concentrations (milligrams per deciliter) were measured at Baseline and after 12 months of treatment/Month 12. Percentage change from Baseline was based on log transformed data and calculated as 100 x (exponent(mean change on log scale) - 1). [Change in Baseline was calculated as Month 12 value (or value after 12 months of treatment) minus the Baseline value.] (NCT00108082)
Timeframe: Baseline and Month 12 (If Month 12 data were not available, the LOCF was used)
Intervention | percentage of change (Geometric Mean) | |||
---|---|---|---|---|
Total cholesterol | Low-density lipid cholesterol | High-density lipid cholesterol | Triglycerides | |
Atenolol | -1.3 | -4.0 | -4.7 | 7.1 |
Carvedilol CR | 0.7 | 0.0 | -4.3 | 11.0 |
Lisinopril | -1.7 | -2.7 | -1.5 | 6.2 |
2 other studies available for carvedilol and Dyslipidemias
Article | Year |
---|---|
Acute and chronic metabolic effects of carvedilol in high-fructose, high-fat diet-fed mice: implication of β-arrestin2 pathway.
Topics: Animals; beta-Arrestin 2; Carvedilol; Diet, High-Fat; Dietary Carbohydrates; Diglycerides; Dyslipide | 2022 |
Cardiovascular risk factors in hypertension: rationale and design of studies to investigate the effects of controlled-release carvedilol on regression of left ventricular hypertrophy and lipid profile.
Topics: Adrenergic beta-Antagonists; Antihypertensive Agents; Carbazoles; Carvedilol; Delayed-Action Prepara | 2006 |