Analyzing Genes That May Increase the Risk of Developing High Blood Pressure
Fine Mapping of Hypertension Genes Detected by Admixture Mapping in the FBPP
2 other identifiers
observational
8,687
1 country
1
Brief Summary
High blood pressure is one of the most common health problems in the United States. Genetic variations may cause some people to be more susceptible to developing high blood pressure. This study will identify variations in genes known to play a part in the development of high blood pressure.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Aug 2007
Longer than P75 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
August 1, 2007
CompletedFirst Submitted
Initial submission to the registry
October 24, 2007
CompletedFirst Posted
Study publicly available on registry
October 26, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2012
CompletedSeptember 10, 2025
September 1, 2025
4.8 years
October 24, 2007
September 4, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Genetic variations
Measured through admixture mapping genetic analysis
Eligibility Criteria
Previously collected genetic samples from African American participants in the Family Blood Pressure Program (FBPP) study and from African American, Mexican American, Nigerian, and Jamaican participants enrolled in other clinical studies will be examined.
You may qualify if:
- Participated in the FBPP study (African American \[800 people with high blood pressure and 800 control group participants\] and Mexican American participants)
- Participated in the American Family Study (African American participants)
- Participated in the Phenotyping Study (African American, Nigerian, and Jamaican participants)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Case Western Reserve University
Cleveland, Ohio, 44106, United States
Biospecimen
Whole blood
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xiaofeng Zhu, PhD
Case Western Reserve University
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 24, 2007
First Posted
October 26, 2007
Study Start
August 1, 2007
Primary Completion
June 1, 2012
Study Completion
June 1, 2012
Last Updated
September 10, 2025
Record last verified: 2025-09