Childhood-Onset Essential Hypertension Natural History Study
Natural History Study to Determine Childhood-Onset Essential Hypertension Etiology
2 other identifiers
observational
2,300
1 country
1
Brief Summary
Background: Childhood-onset essential hypertension (COEH) is high blood pressure that develops in children and teens. High blood pressure is a major risk factor for heart disease. COEH is more likely to be caused by changes in genes rather than by factors like stress or diet. Researchers want to learn more about how changes in genes relate to COEH. They hope to use that information to develop better treatments for children with high blood pressure. Objective: This natural history study will look for genes and gene changes that may lead to COEH. Eligibility: People aged 2 years and older with COEH or who had COEH when they were children. Healthy relatives of those with COEH are also needed. Design: Participants will have one clinic visit per year for up to 10 years. All participants will have a physical exam. They will provide samples of blood and urine. At their first visit, they will have a swab (like a Q-tip) rubbed between their gums and cheeks. They may agree to having a skin biopsy; a piece of skin about the size of a pencil eraser will be removed. Affected participants aged 2 to 17 years old will have additional tests:
- They will have sensors placed on their skin to look at their blood vessels and see how blood is moving in their bodies.
- They will lie or stand while a machine measures the amount of fat and muscle in their bodies.
- They will have an ultrasound; a wand will be rubbed against their skin to take pictures of their kidneys. Other things are optional for all participants:
- They may have photographs taken of their bodies.
- They may have tests of their heart function.
- They may have different types of imaging scans....
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2025
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
First Submitted
Initial submission to the registry
January 15, 2025
CompletedFirst Posted
Study publicly available on registry
January 16, 2025
CompletedStudy Start
First participant enrolled
May 30, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 9, 2034
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 9, 2034
May 27, 2026
May 22, 2026
9.5 years
January 15, 2025
May 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Find all genes that cause COEH.
10 years
Secondary Outcomes (1)
Identify all of the ways that COEH affects the body.
10 years
Study Arms (2)
Affected
Study participants that are 2-17 years old and have COEH or participants that are 18+ years old that were diagnosed with COEH when they were children.
Unaffected
Study participants that are 2+ years old and have never been diagnosed with COEH.
Eligibility Criteria
Study participants will come from hypertension, cardiology, nephrology (kidney), and pediatrician clinics. Participants can also sign themselves up for the study without being referred by their doctor.
You may qualify if:
- To be eligible to participate in this study, an affected individual must meet one of the following criteria:
- Age 2-12 years at time of enrollment with a BP of at least \>95th percentile or 120/80 mm Hg verified via medical record review and a willingness to provide biological samples, undergo physical exam, provide information related to family and medical history, and undergo imaging/body measurements (e.g., renal ultrasound)
- Age 13-17 years at time of enrollment with a BP of at least 130/80 mm Hg verified via medical record review and a willingness to provide biological samples, undergo physical exam, provide information related to family and medical history, and undergo imaging/body measurements (e.g., renal ultrasound)
- To be eligible to participate in this study, an unaffected individual must meet all of the following criteria:
- First-degree relative to a proband (first identified affected family member) in the study
- Willingness to provide biological samples, undergo physical exam, and provide information related to family and medical history
- To be eligible to participate in this study, an individual with a candidate variant (regardless of known COEH status) must meet all of the following criteria:
- History of clinical and/or research genomic interrogation
- Positive genomic interrogation test result for candidate variant identified in earlier stages of study or in prior studies performed by study team
- Willingness to provide information related to family and medical history, provide access to relevant medical records, undergo physical exam, and undergo imaging/body measurements (if 2-17 years of age and evidence of COEH exists)
You may not qualify if:
- An affected individual who meets any of the following criteria will be excluded from participation in this study:
- BMI \>95th percentile
- Evidence that hypertension is secondary to a known condition (e.g., chronic kidney disease, aortopathy, sleep apnea, etc.)
- Impaired decision-making capability, with or without a legally-authorized representative
- An unaffected individual who meets any of the following criteria will be excluded from participation in this study:
- Prior or current diagnosis of COEH
- Second-degree or greater relationship to proband
- Impaired decision-making capability, with or without a legally-authorized representative
- An individual with a candidate variant (regardless of known COEH status) who meets any of the following criteria will be excluded from participation in this study:
- No prior genomic interrogation findings available for the study team to review to confirm positive candidate variant status
- Impaired decision-making capability, with or without a legally-authorized representative
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Neil A Hanchard, M.D.
National Human Genome Research Institute (NHGRI)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- OTHER
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 15, 2025
First Posted
January 16, 2025
Study Start
May 30, 2025
Primary Completion (Estimated)
December 9, 2034
Study Completion (Estimated)
December 9, 2034
Last Updated
May 27, 2026
Record last verified: 2026-05-22
Data Sharing
- IPD Sharing
- Will not share