Serial Serum Samples Investigation for Sepsis and Postresuscitation Therapeutic Strategy
This observational study aims to investigate the relationship between serial serum samples and sepsis, as well as post-resuscitation therapeutic strategies, with the primary focus on evaluating the all-cause mortality rate within one month.
Data Collection
Collected from today forward - ProspectiveCardiovascular Diseases+6
+ Heart Diseases
+ Infections
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: July 1, 2006
Actual date on which the first participant was enrolled.This study focuses on individuals who are in the emergency intensive care unit due to sepsis or postresuscitation state. The main goal is to explore their serum samples, which are the clear liquids that can be separated from clotted blood. By studying these samples, researchers aim to discover a new treatment strategy for these conditions, highlighting the importance of this research in potentially improving patient care. In this observational study, participants' serum samples are collected and studied over time. The primary outcome measured is the all-cause mortality rate within one month. This helps researchers understand the effectiveness of current treatments and identify potential areas for improvement.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.500 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 16 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Seoul National University Hospital
Seoul, South KoreaOpen Seoul National University Hospital in Google Maps