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Characteristics of Renal Blood Flow in AKI Patients in ICU and Its Clinical Significance

Characteristics of Renal Blood Flow in AKI Patients With Sepsis and Its Clinical Significance

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06090773
Enrollment
96
Registered
2023-10-19
Start date
2023-06-01
Completion date
2023-12-30
Last updated
2024-02-09

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

Conditions

Acute Kidney Injury, Renal Artery Blood Flow, Renal Microcirculation, Renal Venous Return

Brief summary

To study the changes in the renal artery and renal vein with renal cortical and medullary microcirculatory blood flow in patients with sepsis; to study the relationship between renal arteriolar and renal vein with renal cortical and medullary microcirculatory blood flow and renal function; and to find the value of ultrasonographic assessment of renal blood flow indices for evaluating prognosis in patients with sepsis.

Interventions

None listed

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years

Inclusion criteria

* Age between 18-85 years old; Control group: patients with non-acute kidney injury after ICU general surgery; Observation group: patients who met the diagnostic criteria of AKI: Scr elevation ≥26.5 umol/L within 48h; Scr elevation exceeding 1.5 times and more than the basal value within 7d; and decrease in urine output (\<0.5 ml/kg/h) with a duration of 6h or more.

Exclusion criteria

* Those who did not meet the inclusion criteria or refused to be enrolled; patients with underlying end-stage renal disease or requiring long-term dialysis; renal transplant patients; patients with other underlying systemic diseases causing renal dysfunction (SCr \> 88.4 umol/L); those who were unable to obtain a clear renal ultrasound view; those with suspected contrast allergy; those with pulmonary arterial systolic blood pressure ≥ 90 mm Hg; and those who were pregnant or breastfeeding women.

Design outcomes

Primary

MeasureTime frameDescription
30-day major renal adverse events30-dayFollow-up of patients with prognostic indicators of renal function within 30 days of enrolment, such as blood creatinine and the need for renal replacement therapy.
Renal artery blood flowDay 1,Day 3,Day 5, Day 7Ultrasound assessment of renal artery resistance index, and renal artery blood flow.
Renal venous returnDay 1,Day 3,Day 5, Day 7Ultrasonographic assessment of renal venous reflux profiles.
renal microcirculationDay 1,Day 3,Day 5, Day 7Evaluation of renal microcirculation by ultrasonography.

Countries

China

Outcome results

None listed

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