NCT07167095

Brief Summary

This retrospective observational study investigates factors associated with 90-day mortality among patients with advanced cancer who present to the emergency department (ED). The study will include stage IV solid tumor patients who visited the ED of Etlik City Hospital between December 2022 and March 2025. Demographic, clinical, and laboratory parameters such as performance status, nutritional and inflammatory markers, and biochemical values will be analyzed. The primary objective is to identify prognostic indicators that predict short-term mortality following ED visits. By establishing risk profiles, the study aims to optimize patient triage, guide timely referral to supportive and palliative care services, and improve overall care strategies for advanced cancer patients in acute settings.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
1,250

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
completed

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 Start

First participant enrolled

December 1, 2022

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2023

Completed
2.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

August 24, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

September 11, 2025

Completed
Last Updated

September 11, 2025

Status Verified

September 1, 2025

Enrollment Period

1 month

First QC Date

August 24, 2025

Last Update Submit

September 3, 2025

Conditions

Keywords

90-Day MortalityEmergency DepartmentPrognostic FactorsPerformance StatusNutritional and Inflammatory MarkersOncology Supportive CarePalliative Care

Outcome Measures

Primary Outcomes (1)

  • 90-Day All-Cause Mortality After Emergency Department Visit

    All-cause mortality within 90 days following presentation to the emergency department among patients with stage IV solid tumors. Mortality status will be confirmed using the hospital information system (HBYS) and the national death registry (e-Nabız). Both in-hospital and out-of-hospital deaths will be included.

    90 days after emergency department visit

Secondary Outcomes (9)

  • In-Hospital Mortality During Emergency Department Visit

    30 days after ED discharge

  • 30-Day Emergency Department Re-admission

    30 days after ED discharge

  • 90-Day Hospital Re-admission Rate

    90 days after ED discharge

  • Correlation between ECOG Performance Status and 90-Day Mortality

    90 days after ED visit

  • Correlation between Body Mass Index (BMI) and 90-Day Mortality

    90 days after ED visit

  • +4 more secondary outcomes

Study Arms (1)

Advanced Cancer Patients Presenting to the Emergency Department

This retrospective cohort includes adult patients (≥18 years) with pathologically confirmed stage IV solid tumors who presented to the emergency department of Etlik City Hospital between December 2022 and March 2025. Patients were eligible if they had received systemic anticancer therapy within the previous 6 months and had complete clinical and laboratory records. Both patients discharged from the ED and those who were admitted or died during the ED visit are included. Data collected include demographic characteristics, performance status, primary tumor type, metastatic sites, reasons for ED admission, laboratory values, and subsequent outcomes. The cohort will be analyzed to identify prognostic factors associated with 90-day mortality, ED re-admissions, and re-hospitalizations.

Other: Retrospective Data Collection and Analysis

Interventions

This intervention refers to retrospective evaluation of clinical and laboratory data of advanced cancer patients who presented to the emergency department between December 2022 and March 2025. Data will be extracted from the hospital information system (HBYS) and national death registry (e-Nabız). Parameters include demographics, ECOG performance status, primary tumor type, metastatic sites, laboratory markers (e.g., NLR, CRP, albumin, LDH), and outcomes such as 90-day mortality, re-admissions, and re-hospitalizations. No experimental treatment, drug, or device is administered as part of the study.

Also known as: Observational Chart Review
Advanced Cancer Patients Presenting to the Emergency Department

Eligibility Criteria

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

The study population consists of adult patients (aged 18 years and older) with stage IV solid tumors who presented to the emergency department of Etlik City Hospital (Ankara, Türkiye) between December 2022 and March 2025. Eligible patients must have received systemic anticancer therapy within the preceding 6 months. Both patients discharged from the ED and those who were hospitalized or who died during their ED visit are included. The estimated enrollment is 1,250 patients.

You may qualify if:

  • Age ≥18 years
  • Pathologically confirmed stage IV (metastatic) solid malignancy
  • Followed at Etlik City Hospital, Department of Medical Oncology
  • Presented to the emergency department between December 2022 and March 2025
  • Either discharged on the same day, admitted to the hospital, or died during the ED visit
  • Received systemic anticancer therapy (chemotherapy, immunotherapy, targeted therapy, or hormonal therapy) within the past 6 months
  • Availability of complete clinical and laboratory data

You may not qualify if:

  • Stage I-III cancer patients
  • Patients not receiving systemic therapy, only palliative/supportive care
  • Patients followed in other oncology centers but presenting to Etlik City Hospital ED
  • Patients with hematologic malignancies (e.g., leukemia, lymphoma, multiple myeloma)
  • Patients with missing clinical or laboratory data

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ankara Etlik City Hospital

Ankara, Yenimahalle, 06210, Turkey (Türkiye)

Location

MeSH Terms

Conditions

NeoplasmsEmergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Oncologist

Study Record Dates

First Submitted

August 24, 2025

First Posted

September 11, 2025

Study Start

December 1, 2022

Primary Completion

January 1, 2023

Study Completion

March 1, 2025

Last Updated

September 11, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations