NCT07765030

Brief 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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
150

participants targeted

Target at P50-P75 for all trials

Timeline
3mo left

Started Aug 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress6%
Aug 2026Nov 2026

First Submitted

Initial submission to the registry

August 7, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

August 10, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 14, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Last Updated

August 14, 2026

Status Verified

August 1, 2026

Enrollment Period

3 months

First QC Date

August 7, 2026

Last Update Submit

August 10, 2026

Conditions

Keywords

Emergency Renal Replacement TherapyHemodialysisContinuous Venovenous HemodiafiltrationAcute Kidney InjuryIn-Hospital Mortality

Outcome Measures

Primary Outcomes (1)

  • In-Hospital Mortality

    Number and proportion of patients who die during the index hospitalization following emergency renal replacement therapy with hemodialysis (HD) or continuous venovenous hemodiafiltration (CVVHDF).

    Up to 30 days from emergency department admission

Secondary Outcomes (3)

  • Emergency Department Mortality

    Up to 1 day from emergency department admission

  • Intensive Care Unit Admission

    Up to 1 day from emergency department admission

  • Renal Replacement Therapy-Related Complications

    Up to 8 hours from emergency department admission

Study Arms (2)

Hemodialysis (HD) Group

Critically ill adult patients who underwent hemodialysis (HD) in the emergency department for an emergency renal replacement therapy indication during the study period.

Procedure: Hemodialysis (HD)Procedure: Continuous Venovenous Hemodiafiltration (CVVHDF)

Continuous Venovenous Hemodiafiltration (CVVHDF) Group

Critically ill adult patients who underwent continuous venovenous hemodiafiltration (CVVHDF) in the emergency department for an emergency renal replacement therapy indication during the study period.

Procedure: Hemodialysis (HD)Procedure: Continuous Venovenous Hemodiafiltration (CVVHDF)

Interventions

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) GroupHemodialysis (HD) Group

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.

Continuous Venovenous Hemodiafiltration (CVVHDF) GroupHemodialysis (HD) Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population will consist of critically ill adult patients aged 18 years or older who were managed in the critical care area of the Emergency Department of Antalya Training and Research Hospital between January 1, 2023, and August 1, 2026, and who underwent emergency renal replacement therapy with hemodialysis (HD) or continuous venovenous hemodiafiltration (CVVHDF). All eligible patients meeting the predefined inclusion and exclusion criteria during the study period will be included using a census sampling approach. Data will be obtained retrospectively from the hospital information management system, electronic medical records, laboratory records, renal replacement therapy records, and clinical follow-up notes. No direct participant recruitment or contact will occur.

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Health Sciences, Antalya Training and Research Hospital

Antalya, konyaaltı, 21090, Turkey (Türkiye)

Location

Related Publications (2)

  • Kim JE, Jeong J, Choi Y, Moon HJ. Utilization of Renal Replacement Therapy and Its Impact on the Emergency Department Length of Stay in South Korean Emergency Medical Centers. Medicina (Kaunas). 2026 Jul 1;62(7):1273. doi: 10.3390/medicina62071273.

    PMID: 42512815BACKGROUND
  • Meersch-Dini M, Abu-Tair M, Bayer M, Brinkmann A, Bellmann R, Brunkhorst F, Custodis F, Czock D, Frey O, Galle J, Hermes C, Joannidis M, John S, Jorres A, Kerz T, Kindgen-Milles D, Koczor M, Kram R, Kuhlmann M, Oppert M, Schlieper G, Schmitz M, Zarbock A, Willam C. Multidisciplinary guidelines on renal replacement therapy in intensive care medicine. Crit Care. 2026 Jan 14;30(1):46. doi: 10.1186/s13054-025-05817-6.

    PMID: 41535952BACKGROUND

MeSH Terms

Conditions

Acute Kidney InjuryRenal Insufficiency

Interventions

Renal DialysisContinuous Renal Replacement Therapy

Condition Hierarchy (Ancestors)

Kidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital Diseases

Intervention Hierarchy (Ancestors)

Renal Replacement TherapyTherapeuticsSorption DetoxificationExtracorporeal CirculationSurgical Procedures, Operative

Central Study Contacts

murat Duyan, ASSOCIATE PROFESSOR

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 7, 2026

First Posted

August 14, 2026

Study Start

August 10, 2026

Primary Completion (Estimated)

November 1, 2026

Study Completion (Estimated)

November 1, 2026

Last Updated

August 14, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared because the study is based on retrospective clinical records containing sensitive patient information. Only anonymized, aggregated study results will be reported.

Locations