HYDROXYZINE-QT: Hydroxyzine and Risk of Prolongation of QT Interval

Sponsor
University Hospital, Caen (Other)
Overall Status
Unknown status
CT.gov ID
NCT02814981
Collaborator
(none)
130
1
23
5.7

Study Details

Study Description

Brief Summary

On 04/30/2015, ANSM (the National Security Agency of Medicines and Health Products) shared an information for general practicioners, pediatricians, anesthesiologists, dermatologists, geriatricians, psychiatrists, community pharmacists and hospital about using hydroxyzine and the associated risk of QT prolongation on the electrocardiogram.

Drugs containing hydroxyzine (the best known and most used is the Atarax®) are used in France in various indications including the treatment of minor manifestations of anxiety, premedication with general anesthesia and the symptomatic treatment of urticaria.

A prolonged QT interval is a known risk factor for occurrence of torsades de pointes which can cause sudden death. We distinguish congenital and acquired long QT interval. The main cause of acquired long QT interval is a drug inhibition of the HERG potassium channel 1. Many drugs have been reported to cause sudden death by prolongation of QT interval and occurrence of torsades de pointes (macrolides, anti -arythmics, some psychotropic ...) The molecules based on hydroxyzine are known to be at risk of prolongation of QT interval in an experimental point of view but is not clearly identified in daily clinical practice. Pharmacology unit of Caen was the first to publish a case of QT prolongation under hydroxyzine . Through this publication, associated with other clinical data, hydroxyzine has been added to the list of drugs that can induce QT prolongation .

Despite these recent recommendations, it does not seem that hydroxyzine prescriptions were changed daily and therefore the risk of QT prolongation persists. We therefore propose the study of the impact of hydroxyzine on the QT interval measured on the electrocardiogram in patients hospitalized at the University Hospital of Caen.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    130 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Hydroxyzine and Risk of Prolongation of QT Interval
    Study Start Date :
    Nov 1, 2015
    Anticipated Primary Completion Date :
    Aug 1, 2017
    Anticipated Study Completion Date :
    Oct 1, 2017

    Outcome Measures

    Primary Outcome Measures

    1. Measure of the corrected QT interval in ms [1 day]

      Measure of corrected QT interval with Bazett and Frediriccia method , in DII and V5.

    Secondary Outcome Measures

    1. Number of Incoming of torsade de pointe [up to 1 month]

      polymorphic ventricular tachycardia with a characteristic illusion of a twisting of the QRS complex

    2. risk of sudden death by ventricular arythmia [up to 1 year]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients hospitalized at the University Hospital of Caen with a new prescription of oral hydroxyzine by their referring doctor.

    • Patient 'stable' in hospital in a health service or surgery.

    • Age > 18 years old.

    Exclusion Criteria:
    • Unstable Patient hospitalized in an intensive care unit or intensive care.

    • Patient refusing participation in the study.

    • Age <18 years old.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Alexandre Joachim Caen Basse Normandie France 14000

    Sponsors and Collaborators

    • University Hospital, Caen

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Caen
    ClinicalTrials.gov Identifier:
    NCT02814981
    Other Study ID Numbers:
    • A15-D44-VOL.27
    First Posted:
    Jun 28, 2016
    Last Update Posted:
    Jun 28, 2016
    Last Verified:
    Jun 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by University Hospital, Caen
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 28, 2016