NCT06778239

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,300

participants targeted

Target at P75+ for all trials

Timeline
103mo left

Started May 2025

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress11%
May 2025Dec 2034

First Submitted

Initial submission to the registry

January 15, 2025

Completed
1 day until next milestone

First Posted

Study publicly available on registry

January 16, 2025

Completed
4 months until next milestone

Study Start

First participant enrolled

May 30, 2025

Completed
9.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 9, 2034

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 9, 2034

Last Updated

May 27, 2026

Status Verified

May 22, 2026

Enrollment Period

9.5 years

First QC Date

January 15, 2025

Last Update Submit

May 23, 2026

Conditions

Keywords

Blood PressurePediatricchildhood hypertensionESSENTIAL HYPERTENSIONHypertension

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

Age2 Years - 99 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

RECRUITING

Related Links

MeSH Terms

Conditions

HypertensionEssential Hypertension

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular Diseases

Study Officials

  • Neil A Hanchard, M.D.

    National Human Genome Research Institute (NHGRI)

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Emilyn C Banfield

CONTACT

Neil A Hanchard, M.D.

CONTACT

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

Locations