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Comparison of Effects of Atorvastatin Versus Rosuvastatin on Cardiac Function in Heart Failure Patients (ASTRO-CHF)

Primary Purpose

Heart Failure With Reduced Ejection Fraction

Status
Unknown status
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Atorvastatin Oral Tablet
Rosuvastatin Oral Tablet
Sponsored by
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure With Reduced Ejection Fraction focused on measuring Atorvastatin, Rosuvastatin, Heart failure

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Either gender,18-65 years of age
  2. Left ventricular ejection fraction <40% as assessed by 2D echocardiography
  3. NYHA class II-III
  4. CHF patients currently optimized on standard treatment for at least 1 month before enrolment and on an OPD basis treatment
  5. Ready to give written informed consent
  6. Willing to comply with the study protocol

Exclusion Criteria:

  1. Known hypersensitivity to statins
  2. NYHA class IV patient
  3. Serum creatinine >3 mg/dl
  4. Significant liver disease: SGOT/SGPT >3 times the upper limit of normal (ULN) or >2.5 times the ULN in symptomatic patients
  5. Patient on an enzyme inducer or inhibitor currently
  6. Any malignancy or patient on chemotherapeutic agents
  7. Pregnant or lactating females
  8. Patients who have participated in another trial within the past 3 months
  9. Patient with uncontrolled diabetes mellitus (HbA1c >7 g%)/ uncontrolled hypertension (BP >140/90 mmHg despite in ≥3 antihypertensive drugs)
  10. Patient with HIV/ HBV / HCV infection

Sites / Locations

  • Postgraduate Institute of Medical Education and Research, ChandigarhRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Atorvastatin arm

Rosuvastatin arm

Arm Description

Tablet Atorvastatin 40mg once daily at bed-time given for 6 months

Tablet Rosuvastatin 20mg once daily at bed-time given for 6 months

Outcomes

Primary Outcome Measures

To compare the effect of atorvastatin and rosuvastatin on LVEF
Change from baseline in Left ventricular ejection fraction (LVEF) measured by 2D Echocardiography after atorvastatin or rosuvastatin treatment
To compare the effect of atorvastatin and rosuvastatin on NT-ProBNP
Change from baseline in NT-ProBNP (cardiac marker) after atorvastatin or rosuvastatin treatment.

Secondary Outcome Measures

To compare the effect of atorvastatin and rosuvastatin on IL-6
Change from baseline in IL-6 levels after atorvastatin or rosuvastatin treatment
To compare the effect of atorvastatin and rosuvastatin on hsCRP
Change from baseline in hsCRP levels after atorvastatin or rosuvastatin treatment.
To compare the effect of atorvastatin and rosuvastatin on Minnesota living with heart failure questionnaire (MLHFQ)
Change from baseline in Minnesota living with heart failure questionnaire (MLHFQ) after atorvastatin or rosuvastatin treatment. MLHFQ consists of 21 questions and each question has a score from 0 to 5. The total score ranges from 0 to 105, with higher scores indicating greater impairment in health related quality of life.
To compare the effect of atorvastatin and rosuvastatin on 6-minute walk test (6MWT)
Change from baseline in 6-minute walk test (6MWT) after atorvastatin or rosuvastatin treatment.
Compare incidence of hospitalization for worsening of heart failure at 6 months in atorvastatin and rosuvastatin group
Incidence of hospitalization due to worsening of heart failure in 6 months in both groups
Compare incidence of adverse events and major adverse events including all-cause mortality, non-fatal MI, stroke in atorvastatin and rosuvastatin group.
Incidence of adverse events including serious adverse events in 6 months in both groups

Full Information

First Posted
September 28, 2021
Last Updated
October 11, 2021
Sponsor
Postgraduate Institute of Medical Education and Research
Collaborators
Indian Council of Medical Research
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1. Study Identification

Unique Protocol Identification Number
NCT05072054
Brief Title
Comparison of Effects of Atorvastatin Versus Rosuvastatin on Cardiac Function in Heart Failure Patients
Acronym
ASTRO-CHF
Official Title
Comparison of Effects of Atorvastatin Versus Rosuvastatin Treatment on Cardiac Function and Inflammation in Patients With Chronic Heart Failure With Reduced Ejection Fraction: A Randomised, Double Blind Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 16, 2019 (Actual)
Primary Completion Date
June 30, 2022 (Anticipated)
Study Completion Date
August 31, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research
Collaborators
Indian Council of Medical Research

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Statins have a protective effect in patients with established heart failure because of their lipid-lowering and pleiotropic effects. There is no randomized controlled trial comparing lipophilic versus hydrophilic statins in these patients (head to head comparison). The best evidence so far is from a meta-analysis in which the authors did an adjusted indirect comparison between lipophilic statins and rosuvastatin and found that lipophilic statins were associated with significantly lower incidence of all-cause mortality, cardiovascular mortality, and hospitalization for worsening heart failure compared to rosuvastatin (hydrophilic statin) among patients with heart failure. So, the investigators plan to conduct a randomized controlled trial comparing the effects of atorvastatin and rosuvastatin on cardiac function in patients with heart failure with reduced ejection fraction.
Detailed Description
HMG CoA reductase inhibitors or Statins have been widely used for primary prevention and secondary prevention of atherosclerotic cardiovascular disease. Also, the protective effect of statins has been observed in patients with established heart failure because of their lipid-lowering and pleiotropic effects. Various randomized and non-randomized clinical trials have evaluated statins like Atorvastatin, Rosuvastatin, Simvastatin, Pitavastatin and reported improved clinical outcomes in patients with heart failure with reduced ejection fraction as well as heart failure with preserved ejection fraction. Similar benefits on improved cardiac function, reduced inflammation, and improved mortality have been seen in small randomized controlled trials (RCTs) with Atorvastatin. The two large RCTs - Controlled Rosuvastatin Multinational Study in Heart Failure (CORONA) and Gruppo Italiano per lo Studio della Sopravvivenza nell'Insufficienza cardiac (GISSI-HF) - which compared Rosuvastatin versus placebo, failed to show statistically significant benefits in mortality outcomes in heart failure patients compared to placebo, although CORONA trial did show a significant reduction in hospital admissions but not on mortality. However, these two large trials only compared one statin i.e rosuvastatin versus placebo; which is a hydrophilic statin. Statin is not a uniform class of drugs. They differ in their pleiotropic effects based on lipophilic nature. There is evidence that lipophilic statins enter cells via passive diffusion and are widely distributed to various tissues including cardiac tissues where it exerts pleiotropic actions whereas uptake of hydrophilic statins is via carrier-mediated mechanisms and is restricted to the liver, thus reduced the capacity of non-lipid effects on extra-hepatic tissues. Currently, there is no RCT comparing lipophilic statin versus hydrophilic statin (head to head comparison). The best evidence so far is from a meta-analysis which is an adjusted indirect comparison between lipophilic statins and rosuvastatin. They found that lipophilic statins were associated with a significantly lower incidence of all-cause mortality, cardiovascular mortality, and hospitalization for worsening heart failure compared to rosuvastatin (hydrophilic statin) among patients with heart failure. So, the investigators plan to conduct a randomized controlled trial comparing the effects of atorvastatin and rosuvastatin on cardiac function and inflammation in patients with heart failure with reduced ejection fraction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure With Reduced Ejection Fraction
Keywords
Atorvastatin, Rosuvastatin, Heart failure

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized, double-blind clinical study
Masking
ParticipantCare ProviderInvestigator
Masking Description
Patients will be randomized to two arms in ratio 1:1 using computer-generated random list. Patients, investigator and care provider will be blinded to the treatment group.
Allocation
Randomized
Enrollment
80 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Atorvastatin arm
Arm Type
Experimental
Arm Description
Tablet Atorvastatin 40mg once daily at bed-time given for 6 months
Arm Title
Rosuvastatin arm
Arm Type
Active Comparator
Arm Description
Tablet Rosuvastatin 20mg once daily at bed-time given for 6 months
Intervention Type
Drug
Intervention Name(s)
Atorvastatin Oral Tablet
Intervention Description
Atorvastatin 40 mg
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin Oral Tablet
Intervention Description
Rosuvastatin 20 mg
Primary Outcome Measure Information:
Title
To compare the effect of atorvastatin and rosuvastatin on LVEF
Description
Change from baseline in Left ventricular ejection fraction (LVEF) measured by 2D Echocardiography after atorvastatin or rosuvastatin treatment
Time Frame
Measurements at enrolment (baseline), 3 month and 6 months
Title
To compare the effect of atorvastatin and rosuvastatin on NT-ProBNP
Description
Change from baseline in NT-ProBNP (cardiac marker) after atorvastatin or rosuvastatin treatment.
Time Frame
Measurements at enrolment (baseline), 3 months and 6 months
Secondary Outcome Measure Information:
Title
To compare the effect of atorvastatin and rosuvastatin on IL-6
Description
Change from baseline in IL-6 levels after atorvastatin or rosuvastatin treatment
Time Frame
Measurements at enrolment (baseline) and 6 months
Title
To compare the effect of atorvastatin and rosuvastatin on hsCRP
Description
Change from baseline in hsCRP levels after atorvastatin or rosuvastatin treatment.
Time Frame
Measurements at enrolment (baseline), 3 month and 6 months
Title
To compare the effect of atorvastatin and rosuvastatin on Minnesota living with heart failure questionnaire (MLHFQ)
Description
Change from baseline in Minnesota living with heart failure questionnaire (MLHFQ) after atorvastatin or rosuvastatin treatment. MLHFQ consists of 21 questions and each question has a score from 0 to 5. The total score ranges from 0 to 105, with higher scores indicating greater impairment in health related quality of life.
Time Frame
Measurements at enrolment (baseline), 3 month and 6 months
Title
To compare the effect of atorvastatin and rosuvastatin on 6-minute walk test (6MWT)
Description
Change from baseline in 6-minute walk test (6MWT) after atorvastatin or rosuvastatin treatment.
Time Frame
Measurements at enrolment (baseline), 3 month and 6 months
Title
Compare incidence of hospitalization for worsening of heart failure at 6 months in atorvastatin and rosuvastatin group
Description
Incidence of hospitalization due to worsening of heart failure in 6 months in both groups
Time Frame
Analysis at 6 months
Title
Compare incidence of adverse events and major adverse events including all-cause mortality, non-fatal MI, stroke in atorvastatin and rosuvastatin group.
Description
Incidence of adverse events including serious adverse events in 6 months in both groups
Time Frame
Analysis at 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Either gender,18-65 years of age Left ventricular ejection fraction <40% as assessed by 2D echocardiography NYHA class II-III CHF patients currently optimized on standard treatment for at least 1 month before enrolment and on an OPD basis treatment Ready to give written informed consent Willing to comply with the study protocol Exclusion Criteria: Known hypersensitivity to statins NYHA class IV patient Serum creatinine >3 mg/dl Significant liver disease: SGOT/SGPT >3 times the upper limit of normal (ULN) or >2.5 times the ULN in symptomatic patients Patient on an enzyme inducer or inhibitor currently Any malignancy or patient on chemotherapeutic agents Pregnant or lactating females Patients who have participated in another trial within the past 3 months Patient with uncontrolled diabetes mellitus (HbA1c >7 g%)/ uncontrolled hypertension (BP >140/90 mmHg despite in ≥3 antihypertensive drugs) Patient with HIV/ HBV / HCV infection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ashish Kakkar, MD, DM
Phone
91-172-2755297
Email
drashishkakkar@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rachna Rohilla, MD
Email
rachna.rohilla20@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ashish K Kakkar
Organizational Affiliation
Postgraduate Institute of Medical Education and Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Postgraduate Institute of Medical Education and Research, Chandigarh
City
Chandigarh
ZIP/Postal Code
160012
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ashish kakkar, MD, DM
Phone
91-172-2755297
Email
drashishkakkar@gmail.com
First Name & Middle Initial & Last Name & Degree
Rachna Rohilla, MD
Email
rachna.rohilla20@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Comparison of Effects of Atorvastatin Versus Rosuvastatin on Cardiac Function in Heart Failure Patients

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