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Randomized Trial to Assess Efficacy of PUFA for the Maintenance of Sinus Rhythm in Persistent Atrial Fibrillation (FORWARD)

Primary Purpose

Atrial Fibrillation

Status
Unknown status
Phase
Phase 3
Locations
Argentina
Study Type
Interventional
Intervention
Omega 3 (n-3 PUFA)
Placebo
Sponsored by
Fundacion GESICA
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Persistent atrial fibrillation

Exclusion Criteria:

  • Contraindications or known hypersensitivity to n-3 PUFA
  • Current treatment with n-3 PUFA for any reason
  • Heart failure NYHA class IV
  • Coronary artery bypass surgery or valve replacement within the past 3 months
  • Planned cardiac procedures
  • Known sick-sinus syndrome
  • Diagnosis of Wolff-Parkinson-White
  • Clinical significant valvular etiologies
  • Presence of arrhythmia associated with an acute reversible condition
  • Advanced chronic lung disease
  • Contraindications for anticoagulation therapy
  • Pregnancy or lactation
  • Any non cardiac illness associated with a life expectancy of < 2 years
  • Treatment with any investigational agent within 3 month before randomization
  • Any condition that in the opinion of the investigator would jeopardize the evaluation of efficacy or safety or be associated with poor adherence to the protocol

Sites / Locations

  • Hospital Alemán
  • Clinica Constituyentes
  • Complejo Medico Policial Churruca Visca
  • Fundacion Favaloro
  • Hospital Evita Pueblo FEDITEC
  • Clinica y Maternidad Colon
  • Hospital Privado de la Comunidad
  • Sanatorio Parque
  • CEMIC (Centro de Educación Médica e Investigaciones Clinicas Norberto Quirno)
  • Clinica Romagosa
  • Hospital José de San Martín
  • Sanatorio Integral IOT
  • Centro Cardiovascular Salta

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

1

2

Arm Description

Omega 3

Outcomes

Primary Outcome Measures

Survival free of atrial fibrillation

Secondary Outcome Measures

Number of patients in sinus rhythm at the time of each study visit
Number of hospitalizations for CV reasons
Number of all-cause hospitalizations
Incidence of TE events
Number of patients who die or with non-fatal thromboembolic events

Full Information

First Posted
January 8, 2008
Last Updated
June 21, 2011
Sponsor
Fundacion GESICA
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1. Study Identification

Unique Protocol Identification Number
NCT00597220
Brief Title
Randomized Trial to Assess Efficacy of PUFA for the Maintenance of Sinus Rhythm in Persistent Atrial Fibrillation
Acronym
FORWARD
Official Title
Randomized, Prospective, Placebo-controlled, Multi-center Study to Test the Efficacy of n-3 PUFA for the Maintenance of Normal Sinus Rhythm in Patients With Persistent Atrial Fibrillation
Study Type
Interventional

2. Study Status

Record Verification Date
June 2011
Overall Recruitment Status
Unknown status
Study Start Date
January 2008 (undefined)
Primary Completion Date
July 2011 (Anticipated)
Study Completion Date
August 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Fundacion GESICA

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To demonstrate that in patients with persistent atrial fibrillation who had recovered normal sinus rhythm and treated with the best recommended therapies, the addition of 1 gram / daily of n-3 PUFA is superior to the corresponding placebo for the maintenance of normal sinus rhythm at one year of follow up.
Detailed Description
Atrial fibrillation (AF) impose a substantial and growing economic burden on health care expenditures. In patients with persistent AF, there are fundamentally two ways to manage the arrhythmia: to restore and maintain sinus rhythm (rhythm control) or to allow AF to continue and ensure that the ventricular rate is controlled (rate control). As it has been stated, it goes without saying that if we could prevent atrial fibrillation (AF) or restore and maintain sinus rhythm in patients suffering from persistent AF, without any penalties due to the unwanted effects of drugs or incomplete suppression of AF and its thromboembolic complications, every physician would do so. Current strategies however, are limited to achieve such desirable goal. In the last years a growing amount of evidence and attention regarding the cardio-protective role of Omega 3 fatty acids (n-3 PUFA) became progressively clear and appealing. Epidemiological studies and randomized controlled trials confirms the role of n-3 PUFA in reducing all cause mortality and cardiovascular events mostly in patients at high cardiovascular risk. These effects seems to be mediated mostly by an anti-arrhythmogenic effect. Basic science confirms and extended clinical observations regarding the antiarrhythmogenic effect of these compounds. Recently both basic research and clinical science suggested a role of n-3 PUFA for the prevention and treatment of supraventricular arrhythmias, particularly AF. The purpose of the study is to show that the addition of n-3 PUFA on the top of the best recommended therapies can improve the maintenance of normal sinus rhythm in patients with persistent atrial fibrillation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
1600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Omega 3
Arm Title
2
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Omega 3 (n-3 PUFA)
Intervention Description
1 gram of n-3 PUFA containing DHA and EPA
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Survival free of atrial fibrillation
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of patients in sinus rhythm at the time of each study visit
Time Frame
12 months
Title
Number of hospitalizations for CV reasons
Time Frame
12 months
Title
Number of all-cause hospitalizations
Time Frame
12 months
Title
Incidence of TE events
Time Frame
12 months
Title
Number of patients who die or with non-fatal thromboembolic events
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Persistent atrial fibrillation Exclusion Criteria: Contraindications or known hypersensitivity to n-3 PUFA Current treatment with n-3 PUFA for any reason Heart failure NYHA class IV Coronary artery bypass surgery or valve replacement within the past 3 months Planned cardiac procedures Known sick-sinus syndrome Diagnosis of Wolff-Parkinson-White Clinical significant valvular etiologies Presence of arrhythmia associated with an acute reversible condition Advanced chronic lung disease Contraindications for anticoagulation therapy Pregnancy or lactation Any non cardiac illness associated with a life expectancy of < 2 years Treatment with any investigational agent within 3 month before randomization Any condition that in the opinion of the investigator would jeopardize the evaluation of efficacy or safety or be associated with poor adherence to the protocol
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hernan C Doval, MD
Organizational Affiliation
Fundacion GESICA
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Gianni Tognoni, MD
Organizational Affiliation
Mario Negri Institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Hugo Grancelli, MD
Organizational Affiliation
Fundacion GESICA
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Sergio Varini, MD
Organizational Affiliation
Fundacion GESICA
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Daniel Nul, MD
Organizational Affiliation
Fundacion GESICA
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Alejandro Macchia, MD
Organizational Affiliation
Fundacion GESICA
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Alemán
City
Caba
State/Province
Buenos Aires
ZIP/Postal Code
1118
Country
Argentina
Facility Name
Clinica Constituyentes
City
Caba
State/Province
Buenos Aires
Country
Argentina
Facility Name
Complejo Medico Policial Churruca Visca
City
Caba
State/Province
Buenos Aires
Country
Argentina
Facility Name
Fundacion Favaloro
City
Caba
State/Province
Buenos Aires
Country
Argentina
Facility Name
Hospital Evita Pueblo FEDITEC
City
Lanus
State/Province
Buenos Aires
Country
Argentina
Facility Name
Clinica y Maternidad Colon
City
Mar del Plata
State/Province
Buenos Aires
Country
Argentina
Facility Name
Hospital Privado de la Comunidad
City
Mar del Plata
State/Province
Buenos Aires
Country
Argentina
Facility Name
Sanatorio Parque
City
Rosario
State/Province
Santa Fe
Country
Argentina
Facility Name
CEMIC (Centro de Educación Médica e Investigaciones Clinicas Norberto Quirno)
City
Ciudad Autonoma de Buenos Aires
Country
Argentina
Facility Name
Clinica Romagosa
City
Cordoba
Country
Argentina
Facility Name
Hospital José de San Martín
City
Corrientes
Country
Argentina
Facility Name
Sanatorio Integral IOT
City
Misiones
Country
Argentina
Facility Name
Centro Cardiovascular Salta
City
Salta
Country
Argentina

12. IPD Sharing Statement

Citations:
PubMed Identifier
23265344
Citation
Macchia A, Grancelli H, Varini S, Nul D, Laffaye N, Mariani J, Ferrante D, Badra R, Figal J, Ramos S, Tognoni G, Doval HC; GESICA Investigators. Omega-3 fatty acids for the prevention of recurrent symptomatic atrial fibrillation: results of the FORWARD (Randomized Trial to Assess Efficacy of PUFA for the Maintenance of Sinus Rhythm in Persistent Atrial Fibrillation) trial. J Am Coll Cardiol. 2013 Jan 29;61(4):463-468. doi: 10.1016/j.jacc.2012.11.021. Epub 2012 Dec 19.
Results Reference
derived
PubMed Identifier
19249410
Citation
Macchia A, Varini S, Grancelli H, Nul D, Laffaye N, Ferrante D, Tognoni G, Doval HC; FORomegaARD investigators. The rationale and design of the FORomegaARD Trial: A randomized, double-blind, placebo-controlled, independent study to test the efficacy of n-3 PUFA for the maintenance of normal sinus rhythm in patients with previous atrial fibrillation. Am Heart J. 2009 Mar;157(3):423-7. doi: 10.1016/j.ahj.2008.10.027. Epub 2009 Jan 8.
Results Reference
derived

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Randomized Trial to Assess Efficacy of PUFA for the Maintenance of Sinus Rhythm in Persistent Atrial Fibrillation

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