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Long Term Cognitive Impact of Pediatric Acute Renal Injury

Long Term Cognitive Impact of Pediatric Acute Renal Injury

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02372734
Enrollment
73
Registered
2015-02-26
Start date
2015-06-30
Completion date
2024-06-26
Last updated
2025-06-06

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

Conditions

Acute Kidney Injury

Brief summary

The research study will investigate the longitudinal cognitive outcomes in subjects admitted as children diagnosed with sepsis who may have had acute kidney injury. Each subject will be contacted 2-15 years after their incident admission in order to solicit responses to a functional and cognitive quality of life survey. Children admitted during the same time frame that did not have kidney injury will also be surveyed.

Detailed description

250 subjects with a prior admission for pediatric sepsis will be contacted 2-15 years following the incident admission in order to complete a survey to assess their overall quality of life. Children will be administered the Pediatric Quality of Life (PedsQL) survey with a parental section to allow for parental response. Adult subjects will take the adult version of the PedsQL.

Interventions

OTHERPediatric Quality of Life (Peds QL) Survey

The subjects will be administered the Peds QL survey. Children will also have a parental section for parental response. This is NOT an interventional study.

Sponsors

American Society of Nephrology
CollaboratorOTHER
University of Florida
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
2 Years to 36 Years
Healthy volunteers
No

Inclusion criteria

* Subjects may be adults or children who were admitted to the hospital with a severe infection between January 1998 to December 2014. * Consent from adult or parent/guardian of child to participate in study. * Assent from subjects between 7 and 17 years of age.

Exclusion criteria

* Failure or inability to complete the survey * Participant is unable to understand written or spoken English * Subjects between 7 and 17 years of age unwilling to assent.

Design outcomes

Primary

MeasureTime frameDescription
Overall health related quality of life score (HRQOL)BaselineScale 0-100

Countries

United States

Outcome results

None listed

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