- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06549101
NLR and Emergency Surgery
December 11, 2024 updated by: University of Chile
Neutrophil-to-Lymphocyte Ratio and Mortality After Emergency Surgery
In the immune system, it has been observed that the preoperative neutrophil-to-lymphocyte ratio (NLR) is an index that reflects the state of inflammation and oxidative stress.
In the perioperative period, NLR has been described as a predictor for patients who will develop renal injury, ischemic stroke, and myocardial injury.
Since preoperative inflammation is a predictor of morbidity and mortality in patients undergoing non-cardiac surgery, a retrospective analysis of the inflammatory status of patients undergoing surgery at the center is proposed.
Study Overview
Status
Completed
Conditions
Detailed Description
A retrospective analysis of patients operated on at the Clinical Hospital of the University of Chile is proposed.
The search will be conducted in the electronic medical records of all patients operated on between January and December 2021, with no exclusion criteria for this analysis.
Demographic data, complications, length of hospital stay, and specific characteristics such as the need for mechanical ventilation, time spent in intermediate care units, and ICU as well as total hospitalization time will be recorded.
For the purpose of this study, the preoperative complete blood count of the patients will be analyzed to search for hematological variables that reflect the state of preoperative systemic inflammation.
Study Type
Observational
Enrollment (Actual)
851
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
-
-
-
Santiago, Chile, 8380456
- Hospital Clinico de la Universidad de Chile
-
-
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
Yes
Sampling Method
Non-Probability Sample
Study Population
Emergency patients operated on at the Clinical Hospital of the University of Chile between January and December 2021
Description
Inclusion Criteria:
- Availability of complete blood count in electronic medical records of all patients operated on between January and December 2021
Exclusion Criteria:
- None
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 |
|---|---|---|
|
NLR
Time Frame: Day of surgery
|
Preoperative neutrophil-to-lymphocyte ratio
|
Day of surgery
|
|
Mortality
Time Frame: 6 months after surgery
|
30 and 180 days mortality
|
6 months after surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Felipe Maldonado, M.D., M. Sc., Hospital Clinico de la Universidad de Chile
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 23, 2022
Primary Completion (Actual)
December 30, 2023
Study Completion (Actual)
December 30, 2023
Study Registration Dates
First Submitted
August 7, 2024
First Submitted That Met QC Criteria
August 7, 2024
First Posted (Actual)
August 12, 2024
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
December 11, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OAIC 37/22
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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