Skip to content

Renin Angiotensin Aldosterone System In Septic Kids

Early Identification of Sepsis-associated Acute Kidney Injury Using Ultrasonography Measurements and Renin and Angiotensin Levels in Children and Adults.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06295393
Acronym
RISK
Enrollment
74
Registered
2024-03-06
Start date
2024-01-24
Completion date
2025-06-01
Last updated
2024-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury Due to Sepsis, Acute Kidney Injury (Nontraumatic), Sepsis

Brief summary

Prospective observational cohort study; pediatric sepsis vs. healthy pediatric subjects and pediatric sepsis with acute kidney injury (AKI) vs without AKI. Blood samples and renal ultrasound will be collected on sequential days for septic subject and one time for the healthy patients. Enzyme-linked immunosorbent assays (ELISA) with be run on serum plasma to compare the renin-angiotensin-aldosterone system (RAAS) between groups.

Detailed description

Prospective observational cohort study; pediatric sepsis vs. healthy pediatric subjects and pediatric sepsis with AKI vs without AKI. Powered to collect 74 patients total (37 sepsis,37 healthy) with enrollment ratio 1:1 and expected different of 50% in renin levels, this provides 80% power at an alpha of 0.05. Sepsis identified as pediatric Sequential Organ Failure Assessment (pSOFA) \>/= 2 + infection and/or Phoenix sepsis criteria. Collecting blood samples on subsequent days of hospitalization. For healthy patients, a one-time blood draw will be obtained . Renal ultrasound will be performed on day 1, 2 and 3 of hospitalization. Blood will be collected and plasma stored at -80 degrees Celsius. Plasma thawed in batches and ELISAs for RAAS components. Demographic data will be collected.

Interventions

None listed

Sponsors

Northwell Health
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* pediatric patients age 1 days - 18 years old with sepsis or age 1 day - 18 years and healthy.

Exclusion criteria

* -pre-existing end stage renal disease (ESRD), chronic renal failure (CRF), home use of angiotensin converting enzyme inhibitor(ACE) or angiotensin receptor blocker(ARB) medications, pre-existing congestive heart failure (CHF), and unrepaired congenital heart disease

Design outcomes

Primary

MeasureTime frameDescription
Difference in serum renin in sepsisFor sepsis cohort point 1 collection within the first 48 hours from of meeting sepsis criteria, point 2: 48-72 hours and point 3: 72-94 hours. For the healthy cohort blood drawn at a single time point up to 24 hoursComparison between healthy and septic subjects serum renin levels

Secondary

MeasureTime frameDescription
Septic induced kidney injury will be associated with alterations in renal blood flowFor sepsis cohort point 1 collection within the first 48 hours from of meeting sepsis criteria, point 2: 48-72 hours and point 3: 72-94 hours.Ultrasound will measure blood flow to kidneys during sepsis and compare with serum levels of RAAS
Aberrations in the renin angiotensin aldosterone system (RAAS) in sepsis versus healthy patientsFor sepsis cohort point 1 collection within the first 48hours from of meeting sepsis criteria, point 2: 48-72 hours and point 3: 72-94hours. For the healthy cohort blood drawn at a single time point.Comparison of RAAS components between sepsis and healthy
Aberrations in the renin angiotensin aldosterone system (RAAS) in sepsis associated acute kidney injuryFor sepsis cohort point 1 collection within the first 48 hours from of meeting sepsis criteria, point 2: 48-72 hours and point 3: 72-94 hours.Comparison of RAAS components between sepsis with and without AKI
Changes in renal blood flow on Ultrasound in SepsisFor sepsis cohort point 1 collection within the first 48 hours from of meeting sepsis criteria, point 2: 48-72 hours and point 3: 72-94 hours.Measuring renal blood flow trend over first three days of sepsis
Renal blood flow and RAAS in sepsisFor sepsis cohort point 1 collection within the first 48 hours from of meeting sepsis criteria, point 2: 48-72 hours and point 3: 72-94hours.Comparison between blood flow by renal ultrasound and components of RAAS
Changes in the components of the RAAS over the first three days in sepsisFor sepsis cohort point 1 collection within the first 48hours from of meeting sepsis criteria, point 2: 48-72 hours and point 3: 72-94hours.Measuring components of RAAS over three days and comparing trend

Countries

United States

Contacts

Primary ContactGrace Fisler, MD
gfisler@northwell.edu203-671-0654

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026