search
Back to results

Ranolazine for Improving Symptoms of Palpitations (RYPPLE)

Primary Purpose

Ischemic Heart Disease

Status
Unknown status
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Ranolazine
Placebo
Sponsored by
University of Roma La Sapienza
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Heart Disease focused on measuring Arrhythmias, palpitations

Eligibility Criteria

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

Inclusion Criteria:

  • Symptoms of palpitations
  • Angiographically-proven coronary artery disease
  • Stable conditions
  • No recent acute coronary syndromes
  • Able to understand and willing to sign the informed consent form
  • Symptomatic patients (palpitation) with stable angina pectoris already on therapy with beta-blockers and/or calcium antagonists.

Exclusion Criteria:

  • Women of child bearing potential patients must demonstrate a negative pregnancy test performed within 24 hours
  • Severe renal failure
  • Severe hepatic failure

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Ranolazine

    Placebo

    Arm Description

    Patients will receive ranolazine 750 mg bid for 30 days

    Patients will receive placebo for 30 days

    Outcomes

    Primary Outcome Measures

    Occurrence of symptoms of palpitations
    Occurrence of symptoms of palpitations

    Secondary Outcome Measures

    Occurrence of arrhythmia in case of symptoms of palpitations
    Definition of presence, number, type and duration of the arrhythmia in case of the patient-reported symptoms of palpitations

    Full Information

    First Posted
    December 15, 2011
    Last Updated
    March 6, 2013
    Sponsor
    University of Roma La Sapienza
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT01495520
    Brief Title
    Ranolazine for Improving Symptoms of Palpitations
    Acronym
    RYPPLE
    Official Title
    Ranolazine for the Treatment of sYmPtoms of PaLpitations in patiEnts With Ischemic Heart Disease - The RYPPLE Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2013
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2014 (undefined)
    Primary Completion Date
    December 2014 (Anticipated)
    Study Completion Date
    December 2016 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Roma La Sapienza

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Patients with ischemic heart disease often report multiple symptoms, including angina and palpitations. Ranolazine has antiarrhythmic effects which are largely a result of the drug's effect on multiple ion channels. It remains unknown, however, whether the favorable effects of ranolazine on symptoms and arrhythmias are maintained over time. Aim of this study is to test the hypothesis that chronic treatment with ranolazine can improve the symptomatic status of patients with ischemic heart disease by reducing the occurrence of palpitations.
    Detailed Description
    Background: Patients with ischemic heart disease often report multiple symptoms, including angina and palpitations. Ranolazine is a novel antianginal and antiischemic drug that reduces intracellular sodium and calcium accumulation during ischemia thus limiting ischemic injury. Furthermore, ranolazine has antiarrhythmic effects which are largely a result of the drug's effect on multiple ion channels. It has previously been shown that treatment with ranolazine can reduce the frequency of supraventricular and ventricular tachycardia in the short term. In a subgroup analysis of the MERLIN-TIMI 36 trial, the continuous ECGs of 6,351 patients were analyzed. The results showed that, in comparison with placebo, treatment with ranolazine resulted in fewer episodes of ventricular tachycardia that lasted 8 beats or longer (5.3% versus 8.3%; P <0.001), and in fewer episodes of supraventricular tachycardia (44.7% versus 55%; P <0.001) and new-onset atrial fibrillation (1.7% versus 2.4%; P=0.08). It remains unknown, however, whether the favorable effects of ranolazine on symptoms and arrhythmias are maintained over time. Purpose: The primary objective of this study is to test the hypothesis that chronic treatment with ranolazine can improve the symptomatic status of patients with ischemic heart disease by reducing the occurrence of palpitations.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Ischemic Heart Disease
    Keywords
    Arrhythmias, palpitations

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Allocation
    Randomized
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Ranolazine
    Arm Type
    Active Comparator
    Arm Description
    Patients will receive ranolazine 750 mg bid for 30 days
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Patients will receive placebo for 30 days
    Intervention Type
    Drug
    Intervention Name(s)
    Ranolazine
    Other Intervention Name(s)
    Ranexa TM, Gilead, US
    Intervention Description
    os, pill, 750 mg, b.i.d., 30 days
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    os, pill, b.i.d., 30 days
    Primary Outcome Measure Information:
    Title
    Occurrence of symptoms of palpitations
    Description
    Occurrence of symptoms of palpitations
    Time Frame
    Up to 30 days
    Secondary Outcome Measure Information:
    Title
    Occurrence of arrhythmia in case of symptoms of palpitations
    Description
    Definition of presence, number, type and duration of the arrhythmia in case of the patient-reported symptoms of palpitations
    Time Frame
    Up to 30 days

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Symptoms of palpitations Angiographically-proven coronary artery disease Stable conditions No recent acute coronary syndromes Able to understand and willing to sign the informed consent form Symptomatic patients (palpitation) with stable angina pectoris already on therapy with beta-blockers and/or calcium antagonists. Exclusion Criteria: Women of child bearing potential patients must demonstrate a negative pregnancy test performed within 24 hours Severe renal failure Severe hepatic failure
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Francesco Pelliccia, MD
    Phone
    +39064997
    Email
    f.pelliccia@mclink.it
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Francesco Pelliccia, MD
    Organizational Affiliation
    University Sapienza
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Ranolazine for Improving Symptoms of Palpitations

    We'll reach out to this number within 24 hrs