Skip to content

Acute Kidney Injury in Upper GI Bleeding Patients

Acute Kidney Injury Following Upper Gastrointestinal Bleeding: Incidence and Predictors

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07636083
Enrollment
200
Registered
2026-06-09
Start date
2026-05-15
Completion date
2027-05-15
Last updated
2026-06-09

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

Conditions

Acute Kidney Injury, Upper Gastrointestinal Bleeding

Keywords

UGIB, AKI, Renal Impairment, Gastrointestinal Hemorrhage, Serum Creatinine, Kidney Function, Variceal Bleeding, Non-variceal Bleeding

Brief summary

This study aims to evaluate the incidence of acute kidney injury (AKI) among patients presenting with acute upper gastrointestinal bleeding (UGIB) at Sohag University Hospitals, and to identify predictors associated with renal impairment in these patients.

Detailed description

Upper gastrointestinal bleeding (UGIB) is a common medical emergency associated with significant morbidity and mortality. Acute kidney injury (AKI) is frequently observed in these patients, mainly due to hypovolemia and renal hypoperfusion. Despite its clinical importance, data regarding AKI incidence and predictors in UGIB patients, particularly in Middle Eastern populations, remain limited. This prospective observational study aims to assess renal function abnormalities and identify predictors of AKI in patients with UGIB, including both variceal and non-variceal causes. The study will also evaluate clinical outcomes such as mortality, hospital stay duration, and need for renal replacement therapy.

Interventions

OTHERObservational assessment

No therapeutic intervention is applied. Patients are managed according to standard hospital care, and data are collected observationally.

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patients aged 18 years or older * Patients presenting with clinical features suggestive of acute upper gastrointestinal bleeding (UGIB), including hematemesis, coffee-ground vomiting, or melena * Diagnosis of UGIB confirmed by upper gastrointestinal endoscopy or strong clinical evidence when endoscopy is not immediately available * Patients admitted to Sohag University Hospitals (medical wards or intensive care unit) * Availability of renal function data, including at least one serum creatinine measurement at admission and serial measurements during hospitalization * Availability of baseline renal function (previous serum creatinine within 3-12 months) or estimable baseline during hospitalization

Exclusion criteria

* Patients with end-stage renal disease (ESRD) on chronic dialysis * Patients with a history of renal transplantation * Patients with advanced chronic kidney disease stage 5 (eGFR \<15 mL/min/1.73 m²) not on dialysis * Patients with lower gastrointestinal bleeding * Patients with incomplete or missing essential renal function data * Patients discharged or deceased within 24 hours of hospital admission * Pregnant patients * Patients with acute kidney injury at presentation due to causes other than UGIB

Design outcomes

Primary

MeasureTime frameDescription
Incidence of Acute Kidney Injury (AKI) According to KDIGO CriteriaFrom hospital admission through hospital discharge, up to 30 daysThe incidence of acute kidney injury (AKI) among patients presenting with acute upper gastrointestinal bleeding (UGIB), defined according to KDIGO criteria based on changes in serum creatinine and/or urine output during hospitalization.

Secondary

MeasureTime frameDescription
Percentage of Patients Developing AKI According to Bleeding EtiologyBaseline (hospital admission) with AKI occurrence assessed through hospital discharge, up to 30 daysComparison of AKI incidence between variceal and non-variceal UGIB patients.
Change in Serum Creatinine ConcentrationThrough hospital discharge, up to 30 daysSerum creatinine concentration (mg/dL) measured at admission and during hospitalization to assess changes in renal function.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 10, 2026