🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT07765030
Starting soon Observational

Clinical Characteristics and In-Hospital Outcomes of Critically Ill Patients Receiving Hemodialysis or Continuous Venovenous Hemodiafiltration in the Emergency Department

NCT07765030 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-08-10
Last updated
2026-08-14

Condition(s) studied

Acute Kidney InjuryKidney Failure, AcuteKidney Failure

Investigational drug(s) / intervention(s)

Hemodialysis (HD)Continuous Venovenous Hemodiafiltration (CVVHDF)

Hemodialysis (HD): Hemodialysis performed in the emergency department as part of routine clinical care in critically ill adult patients with an indication for emergency renal replacement therapy.

Continuous Venovenous Hemodiafiltration (CVVHDF): Continuous venovenous hemodiafiltration performed in the emergency department as part of routine clinical care in critically ill adult patients with an indication for emergency renal replacement therapy.

Study summary

This retrospective observational study aims to evaluate the clinical characteristics and in-hospital outcomes of critically ill adult patients who underwent hemodialysis (HD) or continuous venovenous hemodiafiltration (CVVHDF) in the Emergency Department of Antalya Training and Research Hospital between January 1, 2023, and August 1, 2026.

Medical records will be reviewed to collect information on patient demographics, comorbidities, clinical findings at admission, vital signs, renal replacement therapy indications, laboratory results before and after treatment, treatment modality, treatment-related complications, need for intubation or vasopressor/inotropic support, intensive care unit admission, length of stay, and hospital outcomes.

The primary outcome is in-hospital mortality. Secondary outcomes include emergency department mortality, intensive care unit admission, ward admission, discharge status, emergency department and hospital length of stay, need for intubation or vasopressor/inotropic support, treatment completion, treatment-related complications, and changes in laboratory parameters before and after renal replacement therapy. No additional intervention, test, treatment, or biological sample collection will be performed as part of this study.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age 18 years or older. * Followed in the critical care area of the Emergency Department of Antalya * Training and Research Hospital between January 1, 2023, and August 1, 2026. * Presence of an indication for emergency renal replacement therapy. * Underwent hemodialysis (HD) or continuous venovenous hemodiafiltration (CVVHDF) in the emergency department. * Required critical care-level monitoring or management. * Availability of sufficient demographic, clinical, laboratory, and in-hospital outcome data in the hospital information system, electronic medical records, laboratory records, or clinical follow-up notes. Exclusion Criteria: * Age younger than 18 years. * Renal replacement therapy initiated outside the emergency department. * Presentation only for routine chronic hemodialysis at the hospital dialysis unit without receiving renal replacement therapy in the emergency department. * Renal replacement therapy planned in the emergency department but HD or CVVHDF could not be performed. * Missing essential clinical, laboratory, or in-hospital outcome data. In patients with repeated emergency department admissions, only the first emergency renal replacement therapy episode will be included to reduce statistical dependency.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Health Sciences, Antalya Training and Research Hospital Antalya konyaaltı

More Antalya Health Sciences University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07765030 on ClinicalTrials.gov ↗ ← All trials in Turkey