The Long QT Syndrome in Pregnancy
1 other identifier
observational
12
1 country
1
Brief Summary
Long QT Syndrome (LQTS) is a disease of young adults and can affect women of child bearing age. Suffers of LQTS are at risk of ventricular dysrhythmias including torsades de pointes and ventricular fibrillation. Pregnancy increases the chance that any mother may have an abnormal heart rhythm or arrhythmia. This chance is higher with the LQTS. There are only a few reported cases of women with the LQTS having a baby in the medical literature. This can make it difficult for the doctor caring for a pregnant woman with the long QT syndrome - especially should they need an anesthetic. We would like to study as many women who have had a baby who have the long QT syndrome to give us a better idea of whether there are any arrhythmias occurring at the time of delivery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jun 2007
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2007
CompletedFirst Submitted
Initial submission to the registry
June 18, 2007
CompletedFirst Posted
Study publicly available on registry
June 20, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2008
CompletedApril 14, 2011
April 1, 2011
June 18, 2007
April 12, 2011
Conditions
Keywords
Eligibility Criteria
Women managed at St. Paul's or BC Women's, Vancouver, who have been pregnant in the last 5 years
You may qualify if:
- Pregnant women with diagnoses of Long QT Syndrome, Romano Ward and Jervell - Lange Nielson Syndrome who delivered at BC Women's Hospital or St Paul's Hospital.
You may not qualify if:
- Non consent to participation in the study
- Age less than 19
- Non English speaker
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
BC Women's Hospital
Vancouver, British Columbia, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Roanne Preston, MD
University of British Columbia
- STUDY DIRECTOR
Elizabeth Drake, MD
University of British Columbia
- STUDY DIRECTOR
Joanne Douglas, MD
University of British Columbia
- STUDY DIRECTOR
Marla Kiess, MD
University of British Columbia
- STUDY DIRECTOR
Stanley Tung, MD
University of British Columbia
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
June 18, 2007
First Posted
June 20, 2007
Study Start
June 1, 2007
Study Completion
April 1, 2008
Last Updated
April 14, 2011
Record last verified: 2011-04