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Study of Cardiac and Paroxysmal Abnormalities in Rett Syndrome

Primary Purpose

Rett Syndrome

Status
Completed
Phase
Locations
Study Type
Observational
Intervention
Sponsored by
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an observational trial for Rett Syndrome focused on measuring Rett syndrome, neurologic and psychiatric disorders, rare disease

Eligibility Criteria

0 Years - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Classical Rett syndrome meeting Rett Syndrome Diagnostic Work Group criteria Age-matched girls without neurologic or cardiac problems entered as controls

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    February 24, 2000
    Last Updated
    June 23, 2005
    Sponsor
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
    Collaborators
    Baylor College of Medicine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00004773
    Brief Title
    Study of Cardiac and Paroxysmal Abnormalities in Rett Syndrome
    Study Type
    Observational

    2. Study Status

    Record Verification Date
    January 1997
    Overall Recruitment Status
    Completed
    Study Start Date
    August 1995 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    June 1997 (undefined)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
    Collaborators
    Baylor College of Medicine

    4. Oversight

    5. Study Description

    Brief Summary
    OBJECTIVES: I. Evaluate electrocardiographic parameters, including QT and PR intervals and QRS morphology/duration, across clinical stages in patients with Rett syndrome. II. Characterize abnormalities of cardiac conduction and repolarization. III. Assess arrhythmias, heart rate variability, and autonomic nervous system function in these patients using 24-hour Holter monitoring. IV. Record events believed to represent seizures with video, electroencephalogram (EEG), and polygraph monitoring in patients who have more than 1 clinical seizure every 5 days. V. Characterize these events with respect to clinical manifestations, EEG correlates, and other physiologic data. VI. Determine the frequency of seizures vs. events without electrographic correlates in these patients. VII. Determine whether Rett syndrome patients have characteristic or unique types of seizures and/or an epileptic syndrome.
    Detailed Description
    PROTOCOL OUTLINE: Patients receive an electrocardiogram at baseline and every 6 months for 3 years. Clinical stage II patients undergo 24-hour Holter monitoring on the same schedule; age-matched controls are tested once. A group of patients with more than 1 seizure or possible seizure every 5 days undergo 5-day continuous electroencephalogram/polygraphic/video monitoring, with respiratory effort assessment, end tidal carbon dioxide and oxygen saturation levels, and a seizure log.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Rett Syndrome
    Keywords
    Rett syndrome, neurologic and psychiatric disorders, rare disease

    7. Study Design

    Enrollment
    95 (false)

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    0 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Classical Rett syndrome meeting Rett Syndrome Diagnostic Work Group criteria Age-matched girls without neurologic or cardiac problems entered as controls
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Daniel G. Glaze
    Organizational Affiliation
    Baylor College of Medicine
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    7566458
    Citation
    Glaze DG. Commentary: the challenge of Rett syndrome. Neuropediatrics. 1995 Apr;26(2):78-80. doi: 10.1055/s-2007-979728. No abstract available.
    Results Reference
    background
    PubMed Identifier
    9746669
    Citation
    Glaze DG, Schultz RJ. Rett Syndrome: Meeting the Challenge of This Gender-Specific Neurodevelopmental Disorder. Medscape Womens Health. 1997 Jan;2(1):3.
    Results Reference
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    PubMed Identifier
    8021793
    Citation
    Sekul EA, Moak JP, Schultz RJ, Glaze DG, Dunn JK, Percy AK. Electrocardiographic findings in Rett syndrome: an explanation for sudden death? J Pediatr. 1994 Jul;125(1):80-2. doi: 10.1016/s0022-3476(94)70128-8.
    Results Reference
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    Study of Cardiac and Paroxysmal Abnormalities in Rett Syndrome

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