Study of Cardiac and Paroxysmal Abnormalities in Rett Syndrome
Primary Purpose
Rett Syndrome
Status
Completed
Phase
Locations
Study Type
Observational
Intervention
Sponsored by
About this trial
This is an observational trial for Rett Syndrome focused on measuring Rett syndrome, neurologic and psychiatric disorders, rare disease
Eligibility Criteria
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
NCT ID
NCT00004773
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
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
background
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
background
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Study of Cardiac and Paroxysmal Abnormalities in Rett Syndrome
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