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Multicenter Automatic Defibrillator Implantation Trial - Reduce Inappropriate Therapy (MADIT-RIT)

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ClinicalTrials.gov Identifier: NCT00947310
Recruitment Status : Completed
First Posted : July 28, 2009
Results First Posted : April 18, 2013
Last Update Posted : August 8, 2018
Information provided by (Responsible Party):
Boston Scientific Corporation

Brief Summary:
This study will assess the impact of higher rate cutoffs and longer delays than standard programming on inappropriate therapy in primary prevention ICD and CRT-D patients.

Condition or disease Intervention/treatment Phase
Primary Prevention of Sudden Cardiac Arrest Device: Standard ICD programming Device: High rate cutoff Device: Long delay Not Applicable

Detailed Description:
The purpose of the MADIT-RIT trial is to compare the time to first inappropriate therapy using high rate cutoff and/or long delay in primary prevention patients receiving an ICD or CRT-D device compared to standard programming.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 1500 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Participant)
Primary Purpose: Treatment
Official Title: IDE-Exempt: Multicenter Automatic Defibrillator Implantation Trial - Reduce Inappropriate Therapy
Study Start Date : September 2009
Actual Primary Completion Date : August 2012
Actual Study Completion Date : December 2012

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: A
Standard ICD Programming
Device: Standard ICD programming
Standard ICD programming

Experimental: B
High rate cutoff
Device: High rate cutoff
Programming of a high rate cutoff

Experimental: C
Long ICD duration delay
Device: Long delay
Programming of a prolonged delay

Primary Outcome Measures :
  1. Inappropriate ICD Therapy [ Time Frame: Average of 1.4 years follow-up ]
    First occurance of inappropriate therapy (either anti-tachycardia pacing or shock)

Secondary Outcome Measures :
  1. All-cause Mortality [ Time Frame: Average 1.4 years of follow-up ]
  2. Syncope [ Time Frame: Average of 1.4 years follow-up ]
    First episode of syncope

Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Primary prevention patient with ischemic or non-ischemic heart disease who meets current guidelines for dual-chamber ICD or CRT-D device therapy
  • Patient in sinus rhythm
  • Patient on stable optimal pharmacologic therapy for the cardiac condition or who has developed a recent ICD indication that necessitates ICD therapy concurrent with the optimization of pharmacologic therapy
  • Patient ≥ 21 years of age, or legal representative, willing and capable of giving informed consent

Exclusion Criteria:

  • Patient with an implanted pacemaker or CRT-P
  • Patient with existing ICD or CRT-D device components
  • Patient with a history of VT or VF
  • Patient with permanent or chronic AF, or cardioversion for AF, within the past three calendar months before enrollment
  • Patient with coronary artery bypass graft surgery or percutaneous coronary intervention within the past three calendar months prior to enrollment
  • Patient with enzyme-positive myocardial infarction within the past three calendar months prior to enrollment
  • Patient with angiographic evidence of coronary disease who are candidates for coronary revascularization and are likely to undergo coronary artery bypass graft surgery or percutaneous coronary intervention in the foreseeable future
  • Patient with second or third degree heart block
  • Patient in NYHA Class IV
  • Patient who is pregnant or plans to become pregnant during the course of the trial
  • Patient with irreversible brain damage from preexisting cerebral disease
  • Patient with presence of any disease, other than the patient's cardiac disease, associated with a reduced likelihood of survival for the duration of the trial, e.g., cancer, uremia, liver failure, etc.
  • Patient with chronic renal disease with BUN ≥ 50mg/dl or creatinine ≥ 2.5 mg/dl
  • Patient participating in any other clinical trial
  • Patient unwilling or unable to cooperate with the protocol
  • Patient who lives at such a distance from the clinic that travel for follow-up visits would be unusually difficult
  • Patient who does not anticipate being a resident of the area for the scheduled duration of the trial
  • Patient unwilling to sign the consent for participation
  • Patient whose physician does not allow participation

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00947310

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United States, New York
University of Rochester (Multiple Facilities Participating World Wide)
Rochester, New York, United States, 14642
Sponsors and Collaborators
Boston Scientific Corporation
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Principal Investigator: Arthur J Moss, MD University of Rochester
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Boston Scientific Corporation
ClinicalTrials.gov Identifier: NCT00947310    
Other Study ID Numbers: MADIT-RIT
First Posted: July 28, 2009    Key Record Dates
Results First Posted: April 18, 2013
Last Update Posted: August 8, 2018
Last Verified: March 2013
Keywords provided by Boston Scientific Corporation:
Inappropriate therapy
ICD therapy
Primary prevention
Additional relevant MeSH terms:
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Death, Sudden, Cardiac
Heart Arrest
Heart Diseases
Cardiovascular Diseases
Death, Sudden
Pathologic Processes