- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06712134
The Factors Associated 30-day Mortality After Perioperative Cardiac Arrest in Adults Undergoing Non-cardiac Surgery.
November 29, 2024 updated by: Pattrapun Wongsripuemtet, Siriraj Hospital
The Factors Associated 30-day Mortality After Perioperative Cardiac Arrest in Adults Undergoing Non-cardiac Surgery: A 7-year Observational Study From a Tertiary Care University Hospital
Perioperative cardiac arrest (PCA) in patients undergoing noncardiac surgery is a rare but potentially catastrophic event associated with high mortality.
Several studies have highlighted the factors contributing to PCA in the surgical population.
However, information on outcomes after PCA among the surgical population is still limited.
Our study aims to identify the incidence of PCA, 30-days mortality and the factors associated with PCA and 30-day mortality after PCA in adults undergoing non-cardiac surgery
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
105
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients >eighteen years that had non-cardiac surgery under anesthesia and a history of PCA between January 2015 and December 2021 were eligible for inclusion.
Patients with a do not resuscitate (DNR) order, who did not receive cardiopulmonary resuscitation (CPR) during PCA, or with incomplete data regarding 30-day mortality were excluded.
PCA was defined as the absence of mechanical heart function (determined by a central pulse) and loss of effective circulation between the administration of anesthesia until 24 hours after surgery
Description
Inclusion Criteria:
- patients aged> 18 years old
- history of perioperative cardiac arrest
- non- cardiac surgery
Exclusion Criteria:
- did not receive cardiopulmonary resuscitation (CPR) during PCA
- incomplete data regarding 30-day mortality were excluded
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 |
|---|---|---|
|
incidence of 30 days mortality after perioperative cardiac arrest
Time Frame: 30 days
|
incidence of 30 days mortality after perioperative cardiac arrest
|
30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
January 1, 2015
Primary Completion (Actual)
December 31, 2021
Study Completion (Actual)
December 31, 2021
Study Registration Dates
First Submitted
November 26, 2024
First Submitted That Met QC Criteria
November 26, 2024
First Posted (Actual)
December 2, 2024
Study Record Updates
Last Update Posted (Estimated)
December 4, 2024
Last Update Submitted That Met QC Criteria
November 29, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 321/2022
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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