- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06558487
The Internal Prospective Validation of the Cancer Admission Score (CAS) Prediction Model (ONCOMING)
The Internal Prospective validatiON of a prediCtiOn Model for the Change of admIssion for Patient With caNcer Admitted to the emerGency Department (ONCOMING Study)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The goal of this single center prospective observational study is to determine the agreement between the cancer admission score (CAS) predicted disposition and the actual disposition in patients with an active cancer diagnosis visiting the emergency department (ED). The main question it aims to answer are: Is the performance of the CAS good enough to play a potential role in the ED care process.
The first part of this study is an observational part. For patients with cancer that are presented to the emergency department (ED) the cancer admission score (CAS) will be calculated by the model both after triage and after the first blood results are in. Furthermore, the expected disposition will be asked to the attending nurse after triage and after the first blood results. Finally, the actual disposition will be written down after the patient has left the ED, in combination with ED length of stay (LOS) and the time for the attending physician to reach a decision about the disposition (time-to-disposition) and the time for a patient to leave the ED (time-to-leave).
The second part is the interventional part. In this part we introduce an early bed reservation intervention. The CAS is still calculated for the patient. If the CAS is 80% or higher based on the triage, the attending physician will be alerted and a call to the bed coordinator will be placed to reserve a bed in advance. After the first blood results are known the second CAS will be calculated, if this drops below 70% the reserved bed can be canceled by the attending physician. Similar to the first part, the expected disposition from the attending nurse after triage and after first blood results will be collected. Finally, the actual disposition, ED LOS, time-to-disposition and time-to-leave will be noted.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Jason den Duijn
- Phone Number: 0107040704
- Email: j.denduijn@erasmusmc.nl
Study Locations
-
-
Zuid-Holland
-
Rotterdam, Zuid-Holland, Netherlands, 3015GD
- Recruiting
- Erasmus University Medical Center
-
Contact:
- Jason den Duijn, MSc.
- Phone Number: +31107040704
- Email: j.denduijn@erasmusmc.nl
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with solid or hematological malignancies and receiving systemic therapy or having received systemic therapy within the last 3 months.
- Presented at or admitted from the emergency department for the oncology, hematology neuro- or lung-oncology clinical unit.
Exclusion Criteria:
- <18 years old
- Only received a surgical intervention as cancer treatment
- Admitted to the ED for the surgical department
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Cancer patients
All adult patients with an active cancer diagnosis who visit the emergency department (ED) of the Erasmus University Medical Centre (Erasmus MC).
|
A prediction model that calculates the chance for a patient to be admitted after triage and after first blood results
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Disposition
Time Frame: Through study completion, an average of 6 months
|
The outcome of a visit to the ED, being either admission or home
|
Through study completion, an average of 6 months
|
|
Agreement between the CAS and the actual disposition
Time Frame: Through study completion, an average of 6 months
|
Agreement between the CAS predicted outcome and the actual outcome
|
Through study completion, an average of 6 months
|
|
Cancer Admission Score
Time Frame: Through study completion, an average of 6 months
|
Cancer Admission Score (CAS) calculated after triage and after first blood results, ranging from 0 to 100%.
The higher the score the greater the change of admission
|
Through study completion, an average of 6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Agreement between expected disposition by nurse and actual disposition
Time Frame: Through study completion, an average of 6 months
|
Agreement between the nurse predicted outcome and the actual outcome
|
Through study completion, an average of 6 months
|
|
time-to-disposition
Time Frame: Through study completion, an average of 6 months
|
The average time between patient's arrival at the emergency department (ED) and the decision to disposition
|
Through study completion, an average of 6 months
|
|
time-to-leave
Time Frame: Through study completion, an average of 6 months
|
The average time between the decision to disposition and departure from the ED (either home or ward)
|
Through study completion, an average of 6 months
|
|
ED Length of Stay
Time Frame: Through study completion, an average of 6 months
|
The total time spent in the ED by a patient during their visit
|
Through study completion, an average of 6 months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sex
Time Frame: Through study completion, an average of 6 months
|
The sex of a patient
|
Through study completion, an average of 6 months
|
|
Age
Time Frame: Through study completion, an average of 6 months
|
The age of a patient
|
Through study completion, an average of 6 months
|
|
Type of Cancer
Time Frame: Through study completion, an average of 6 months
|
The type of cancer a patient has
|
Through study completion, an average of 6 months
|
|
Type of Treatment
Time Frame: Through study completion, an average of 6 months
|
Type of cancer treatment a patient receives
|
Through study completion, an average of 6 months
|
|
Main Complaint
Time Frame: Through study completion, an average of 6 months
|
Main complaint of ED visit
|
Through study completion, an average of 6 months
|
|
Physical parameters recorded during triage
Time Frame: Through study completion, an average of 6 months
|
Physical parameters that are recorded during triage and are used in the prediction model
|
Through study completion, an average of 6 months
|
|
First Blood results
Time Frame: Through study completion, an average of 6 months
|
The blood results that are recorded during triage and are used in the prediction model
|
Through study completion, an average of 6 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jason den Duijn, Erasmus Medical Center
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 12821
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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