Prevalence and Clinical Characteristics of Obesity Hypoventilation Syndrome in Critically Ill Obese Patients
This study aims to observe and determine the prevalence of obesity hypoventilation syndrome among critically ill Asian patients with a Body Mass Index (BMI) of 30 kg/m² or higher in intensive care units.
Data Collection
Collected from today forward - ProspectiveApnea+14
+ Hypoventilation
+ Nervous System Diseases
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: October 29, 2014
Actual date on which the first participant was enrolled.This study focuses on a health condition called Obesity Hypoventilation Syndrome (OHS), which affects individuals who are obese, specifically those with a Body Mass Index (BMI) of 30 kg/m2 or higher. The research is conducted in medical intensive care units, targeting adult patients who have recently been admitted and diagnosed with OHS. The main goal is to understand how common this condition is among critically ill patients and to identify factors that might predict its occurrence, thereby improving care and addressing current challenges in managing OHS. The study is observational in nature, meaning participants will undergo routine medical care while their health is closely monitored. Researchers will screen for OHS among obese patients in the intensive care unit, observing its prevalence in this specific population. The primary outcome measured is the prevalence of OHS among Asian critically ill patients. This will be achieved by screening for obesity (BMI>=30kg/m^2) in critical care units, providing valuable insights into the condition's prevalence in the Asian population.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.52 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.From 20 to 80 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.Study Objectives
Primary 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
National Taiwan University Hospital
Taipei, TaiwanOpen National Taiwan University Hospital in Google Maps