Ivabradine in Cirrhotic Cardiomyopathy
Primary Purpose
Cirrhotic Cardiomyopathy, Left Ventricular Dysfunction, Cirrhosis, Liver
Status
Recruiting
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Betablocker + ivabradine
Betablocker
Sponsored by
About this trial
This is an interventional treatment trial for Cirrhotic Cardiomyopathy focused on measuring Cirrhotic cardiomyopathy, Left ventricular diatolic dysfunction, Carvedilol, Ivabradine
Eligibility Criteria
Inclusion Criteria:
- Age range of 18-65 years
- Cirrhosis, as diagnosed by histology or clinical, laboratory and USG findings,
- LV diastolic dysfunction on 2D echocardiography
Exclusion Criteria:
- Chronic renal disease
- Patient already on beta blocker
- Pregnancy and peripartum cardiomyopathy
- Hypertension
- Coronary artery disease
- Valvular heart disease
- Sick sinus syndrome/ Pacemaker
- Cardiac rhythm disorder
- Hypothyroidism
- Hyperthyroidism
- Portal vein thrombosis
- Transjugular intrahepatic porto systemic shunt (TIPS) insertion
- Hepatocellular carcinoma
- Anemia Hb < 8gm/dl in females, and < 9 gm/dl in males
Sites / Locations
- Postgraduate Institute of Medical Education and ResearchRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Carvedilol + Ivabradine
Carvedilol
Arm Description
Outcomes
Primary Outcome Measures
Survival
All cause mortality to be assessed
Secondary Outcome Measures
Change in E/e' Ratio
Echo parameter to be documented
Change in renal function
Change in HRQoL
Change in neurohormonal markers- Brain natriuretic peptide, aldosterone, plasma renin activity
Number of Episodes of Cirrhosis related events
New onset ascites, variceal bleeding,hepatorenal syndrome
Full Information
NCT ID
NCT04111133
First Posted
September 26, 2019
Last Updated
September 19, 2023
Sponsor
Postgraduate Institute of Medical Education and Research
1. Study Identification
Unique Protocol Identification Number
NCT04111133
Brief Title
Ivabradine in Cirrhotic Cardiomyopathy
Official Title
Efficacy of Carvedilol + Ivabradine vs Carvedilol Alone for Left Ventricular Diastolic Dysfunction in Chronic Liver Disease Patients and Its' Impact on Morbidity and Mortality; a Prospective Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A total of 130 patients with liver cirrhosis who fulfill the criteria of the study, and who have been found to have left ventricular diastolic dysfunction on a screening 2D echocardiography, will then be randomized by Block randomization technique, to two arms in a ratio 1:1(Group A) will receive carvedilol+ Ivabradine targeted therapy for heart rate reduction while Group B will receive Carvedilol alone; and the dosage of drug in the treatment arm will be titrated every week to achieve target heart rate of 50-60/ minute. Patients in the treatment arms, who are unable to tolerate carvedilol due to hypotension episodes, will be offered ivabradine alone to allow achievement of targeted heart rate reduction. All patients will be evaluated at 0,6, and 12 months. The end points will be clinical events, cardiac function improvement, renal function, and mortality.
Detailed Description
The investigators have already demonstrated the role of targeted heart rate reduction in the management of LVDD in cirrhosis, but the previous study could not demonstrate the role of ivabradine alone in absence of betablocker therapy. This trial will be a validation cohort for the initial data obtained on this novel drug. The use of ivabradine can treat patients who do not tolerate betablocker therapy due to contraindications or adverse effects especially hypotension.
Diagnosis of CCM will be as per 2020 CCMC criteria. CCM is defined as systolic or diastolic dysfunction in the absence of alternative cardiac pathology in concordance with the Cirrhotic Cardiomyopathy Consortium (CCMC) criteria. 9 Systolic dysfunction was defined as an ejection fraction (EF) ≤50% or an absolute value of GLS <18%. CCM will defined as presence of 3 of the following 4 criteria: septal early diastolic mitral annular flow velocity (e') <7 cm/s, early diastolic transmitral flow to early diastolic mitral annular velocity (E/e') ≥15, left atrial volume index (LAVI) >34 mL/m2, tricuspid jet maximum velocity >2.8 m/s, in the absence of pulmonary hypertension and the presence of measurable early to late diastolic transmitral flow velocity (E/A) ratio (E/A >2 = grade 3 & E/A 0.8-2 = grade 2 LVDD). Persons meeting only 2 criteria will be termed as indeterminate for LVDD grade.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhotic Cardiomyopathy, Left Ventricular Dysfunction, Cirrhosis, Liver, Portal Hypertension
Keywords
Cirrhotic cardiomyopathy, Left ventricular diatolic dysfunction, Carvedilol, Ivabradine
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Open Label
Allocation
Randomized
Enrollment
130 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Carvedilol + Ivabradine
Arm Type
Experimental
Arm Title
Carvedilol
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Betablocker + ivabradine
Intervention Description
Use of maximum tolerated dose of carvedilol and ivabradine to achieve therapeutic heart rate reduction (THR) to 55-65 beats per minute
Intervention Type
Drug
Intervention Name(s)
Betablocker
Intervention Description
Use of maximum tolerated dose of carvedilol to achieve targeted heart rate reduction (THR) to 55-65 beats per minute (responder) or inability to reach THR (non responder) with maximum dose of carvedilol, maintaining a minimum MAP of 70 mmHg.
Primary Outcome Measure Information:
Title
Survival
Description
All cause mortality to be assessed
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Change in E/e' Ratio
Description
Echo parameter to be documented
Time Frame
12 months
Title
Change in renal function
Time Frame
12 months
Title
Change in HRQoL
Time Frame
12 months
Title
Change in neurohormonal markers- Brain natriuretic peptide, aldosterone, plasma renin activity
Time Frame
12 months
Title
Number of Episodes of Cirrhosis related events
Description
New onset ascites, variceal bleeding,hepatorenal syndrome
Time Frame
12 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:
Age range of 18-65 years
Cirrhosis, as diagnosed by histology or clinical, laboratory and USG findings,
LV diastolic dysfunction on 2D echocardiography
Exclusion Criteria:
Chronic renal disease
Patient already on beta blocker
Pregnancy and peripartum cardiomyopathy
Hypertension
Coronary artery disease
Valvular heart disease
Sick sinus syndrome/ Pacemaker
Cardiac rhythm disorder
Hypothyroidism
Hyperthyroidism
Portal vein thrombosis
Transjugular intrahepatic porto systemic shunt (TIPS) insertion
Hepatocellular carcinoma
Anemia Hb < 8gm/dl in females, and < 9 gm/dl in males
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Madhumita Premkumar, MD DM
Phone
01722756344
Email
drmadhumitap@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Radha K Dhiman, MD DM
Organizational Affiliation
Postgraduate Institute of Medical Education and Research
Official's Role
Study Chair
Facility Information:
Facility Name
Postgraduate Institute of Medical Education and Research
City
Chandigarh
State/Province
Choose Any State/Province
ZIP/Postal Code
160012
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Madhumita Premkumar
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
31342529
Citation
Izzy M, VanWagner LB, Lin G, Altieri M, Findlay JY, Oh JK, Watt KD, Lee SS; Cirrhotic Cardiomyopathy Consortium. Redefining Cirrhotic Cardiomyopathy for the Modern Era. Hepatology. 2020 Jan;71(1):334-345. doi: 10.1002/hep.30875. Epub 2019 Oct 11. Erratum In: Hepatology. 2020 Sep;72(3):1161.
Results Reference
result
PubMed Identifier
31305281
Citation
Premkumar M, Rangegowda D, Vyas T, Khumuckham JS, Shasthry SM, Thomas SS, Goyal R, Kumar G, Sarin SK. Carvedilol Combined With Ivabradine Improves Left Ventricular Diastolic Dysfunction, Clinical Progression, and Survival in Cirrhosis. J Clin Gastroenterol. 2020 Jul;54(6):561-568. doi: 10.1097/MCG.0000000000001219.
Results Reference
result
PubMed Identifier
35068798
Citation
Kaur H, Premkumar M. Diagnosis and Management of Cirrhotic Cardiomyopathy. J Clin Exp Hepatol. 2022 Jan-Feb;12(1):186-199. doi: 10.1016/j.jceh.2021.08.016. Epub 2021 Aug 21.
Results Reference
result
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Ivabradine in Cirrhotic Cardiomyopathy
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