- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07588204
Non Urgent Visit to Emergency Department
May 11, 2026 updated by: Seethalakshmi Avudaiappan, Sri Ramachandra Institute of Higher Education and Research
Non Urgent Visit to Emergency Department at a Tertiary Care Hospital - A Retrospective Analysis
The use of ED by patients with non-urgent conditions has largely been seen in many hospitals.
However, in general, half of the patients who visit the ED are non-urgent conditions.
Due to this, the ED continues to struggle with overcrowding.
This study aimed to determine the common reasons for non-urgent visits and their management in the ED by analysing the past medical records between January 2024 to December 2024.
The management includes triage time, consultation time, cross referrals, and time taken by cross referrals, admission and discharge status, admission and discharge criteria, time taken for admission and discharge decisions, and delay time and reason for delay.
Study Overview
Status
Completed
Detailed Description
Nurses must understand emergency department flow and patient management patterns to effectively interact with patients who present with varied healthcare needs.
This retrospective study was conducted at Sri Ramachandra Medical Centre to evaluate non-urgent visits to the Emergency Department.
Data was collected from medical records (case sheets) of ER patient admissions between January 2024 to December 2024.
The study focused on patients who were in the non-urgent (triage) category, excluding urgent category patients.
The study analyzed triage management including triage time, consultation time, cross referrals, admission and discharge status and criteria, time taken for decisions, and reasons for delay.
Study Type
Observational
Enrollment (Actual)
29856
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Tamil Nadu
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Chennai, Tamil Nadu, India, 600116
- Sri Ramachandra Institute of Higher Education and Research
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Medical records of patients attending the emergency department for non urgent complaints
Description
Inclusion Criteria:
- Medical records of Emergency department patient admissions between January 2024 to December 2024
- Records of patients who were classified as non-urgent triage category
Exclusion Criteria:
- Medical records of patients who were classified in the urgent category
- Incomplete or missing data in the medical records
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Triage Management Patterns
Time Frame: Medical records from January 2024 to December 2024
|
Analysis of time taken for management
|
Medical records from January 2024 to December 2024
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Delay Analysis
Time Frame: Medical records from January 2024 to December 2024
|
Identification of delay time and reasons for delay in non-urgent ED visits
|
Medical records from January 2024 to December 2024
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Seethalakshmi Avudaiappan, Sri Ramachandra Institute of Higher Education and Research
- Principal Investigator: Shivasankari Selvaraj Lakshmi, M.Sc Nursing, Sri Ramachandra Institute of Higher Education and Research
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2025
Primary Completion (Actual)
October 20, 2025
Study Completion (Actual)
October 20, 2025
Study Registration Dates
First Submitted
April 27, 2026
First Submitted That Met QC Criteria
May 11, 2026
First Posted (Actual)
May 14, 2026
Study Record Updates
Last Update Posted (Actual)
May 14, 2026
Last Update Submitted That Met QC Criteria
May 11, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- NUR/160/197
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Individual participant data will not be publicly shared.
De-identified data may be available from the corresponding investigator upon reasonable request.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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