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Efficacy Study of Digoxin & Ivabradine to Treat Heart Failure (Dig&Iva)

Primary Purpose

Cardiac Failure

Status
Completed
Phase
Phase 4
Locations
Switzerland
Study Type
Interventional
Intervention
Ivabradine
Digoxin
Sponsored by
Cocco, Giuseppe, M.D.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Failure focused on measuring Digoxin, Ivabradine, with atrial fibrillation.

Eligibility Criteria

60 Years - 78 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

All patients had heart failure NYHA (New York Heart Association) class III. All had chronic and stable coronary artery disease which had been treated with percutaneous dilatation and stenting, and/or aortocoronary bypass. The pathology had induced a permanent AF and heart failure with left ventricular diastolic dysfunction and preserved systolic function. Preserved systolic function was defined by a LVEF (left ventricular ejection fraction) ≥52%. Left ventricular diastolic dysfunction was defined by a e/e1 ratio > 15 (septal spectral tissue-Doppler).

Exclusion Criteria:

Unstable myocardial ischemia, reduced systolic cardiac function (LVEF<52%), diabetes mellitus requiring insulin, moderate or severe renal or hepatic dysfunction, or technically insufficient echocardiography.

Sites / Locations

  • Cardiology office

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Ivabradine

Digoxin

Arm Description

Ivabradine, 7,5 mg b.id. by mouth for 14-16 weeks.

Digoxin 0.125 mg once a day, 5 times per week, for 12-14 weeks by mouth.

Outcomes

Primary Outcome Measures

Comparative therapeutic effect.
Effects on symptoms and signs of cardiac failure.

Secondary Outcome Measures

Full Information

First Posted
September 12, 2012
Last Updated
November 8, 2013
Sponsor
Cocco, Giuseppe, M.D.
Collaborators
Cardiology Office, Rheinfelden, Switzerland
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1. Study Identification

Unique Protocol Identification Number
NCT01699776
Brief Title
Efficacy Study of Digoxin & Ivabradine to Treat Heart Failure
Acronym
Dig&Iva
Official Title
Comparison of Digoxin and Ivabradine in Heart Failure With Preserved Systolic Function. Time to Rethink About Digoxin.
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
April 2008 (undefined)
Primary Completion Date
February 2012 (Actual)
Study Completion Date
February 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cocco, Giuseppe, M.D.
Collaborators
Cardiology Office, Rheinfelden, Switzerland

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
It is established that at a serum concentration 0.5-0.9 ng/ml digoxin is effective in patients with heart failure, especially in the presence of atrial fibrillation (AF). It is the claimed that ivabradine by lowering heart rate reduces symptoms and improves clinical outcomes in patients with heart failure. The effect of ivabradine and digoxin in heart failure was compared. Patients 22 patients with ischemic heart failure, AF, and diastolic dysfunction with preserved left ventricular systolic function were treated with digoxin and ivabradine for 3 months, according to a randomization cross-over design. Collected data Medical history, physical examination, laboratory (including proBNP and serum digoxin concentrations), ECG, 6-minute walk test, and echocardiographic data (LVEF, LAVi, e/e1 ratio).
Detailed Description
Protocol This is an investigator-started study, coded GC&PJ-dig-Iva 2009-2012. The study was planned according to the Good Clinical Quality standards and the analysis was performed using an intention-to-treat method. The protocol was approved from an Ethics Committee. Selected patients gave their written informed consent. The family practitioners agreed and obtained the data and analysis. Collected data were analyzed from single-blinded investigators (without knowledge of the used test drug and time of collection). Patients Study design: same patients were assigned to DIG or IVA for 3 months, according to a randomization cross-over design. Tested drugs Commercial brands of digoxin and ivabradine were used. Digoxin was given by mouth at a dose of 0.125 mg/day, 5 times per week, for 3 months. Ivabradine was given by mouth at a dose of 7.5 mg bid for 3 months. Inclusion criteria Chronic and stable coronary artery disease Permanent atrial fibrillation. Diastolic dysfunction with maintained systolic function. Exclusion criteria Unstable angina pectoris. Reduced systolic cardiac function (LVEF<52%). Normal diastolic function. Diabetes requiring insulin. Moderate or severe renal or hepatic dysfunction. Technically insufficient echocardiographic quality. Collected data Medical history and concomitant medications. Physical examination was performed. Laboratory values (including proBNP and serum digoxin concentration). ECG. Echocardiography. 6-minute walk test. Statistical Analyses Data are expressed as mean ± 1 SD. Absolute values and percent changes in relation to baseline measurements were analyzed. The 2 hypotheses tested were: null hypothesis: mu1-mu2=0.0, and alternative hypothesis: mu1-mu2>>0.0. Comparisons within groups were made using paired t tests or the non-parametric Wilcoxon signed-rank test, where appropriate. Between-group comparisons were performed by unpaired t tests or the non-parametric Mann-Whitney U test, respectively. Chi-square test or Kruskal-Wallis test were used to compare continuous normally or not normally distributed and qualitative variables, where appropriate. Multivariate analysis of variance was performed. A p value of < 0.05 was considered statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Failure
Keywords
Digoxin, Ivabradine, with atrial fibrillation.

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
22 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ivabradine
Arm Type
Active Comparator
Arm Description
Ivabradine, 7,5 mg b.id. by mouth for 14-16 weeks.
Arm Title
Digoxin
Arm Type
Active Comparator
Arm Description
Digoxin 0.125 mg once a day, 5 times per week, for 12-14 weeks by mouth.
Intervention Type
Drug
Intervention Name(s)
Ivabradine
Other Intervention Name(s)
Procoralan
Intervention Description
7.5 my b.id. by mouth for 12-14 weeks
Intervention Type
Drug
Intervention Name(s)
Digoxin
Intervention Description
1.25 mg once a day by mouth, for 12-14 weeks.
Primary Outcome Measure Information:
Title
Comparative therapeutic effect.
Description
Effects on symptoms and signs of cardiac failure.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
78 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients had heart failure NYHA (New York Heart Association) class III. All had chronic and stable coronary artery disease which had been treated with percutaneous dilatation and stenting, and/or aortocoronary bypass. The pathology had induced a permanent AF and heart failure with left ventricular diastolic dysfunction and preserved systolic function. Preserved systolic function was defined by a LVEF (left ventricular ejection fraction) ≥52%. Left ventricular diastolic dysfunction was defined by a e/e1 ratio > 15 (septal spectral tissue-Doppler). Exclusion Criteria: Unstable myocardial ischemia, reduced systolic cardiac function (LVEF<52%), diabetes mellitus requiring insulin, moderate or severe renal or hepatic dysfunction, or technically insufficient echocardiography.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giuseppe Cocco, MD
Organizational Affiliation
Cardiologist, senior lecturer
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cardiology office
City
Rheinfelden
State/Province
Argovia
ZIP/Postal Code
CH-4310
Country
Switzerland

12. IPD Sharing Statement

Citations:
PubMed Identifier
24765517
Citation
Cocco G, Jerie P. Comparison between ivabradine and low-dose digoxin in the therapy of diastolic heart failure with preserved left ventricular systolic function. Clin Pract. 2013 Nov 4;3(2):e29. doi: 10.4081/cp.2013.e29. eCollection 2013 Aug 2.
Results Reference
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Efficacy Study of Digoxin & Ivabradine to Treat Heart Failure

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