Sedation, ANalgesia and Delirium MANagement in Intensive Care Unit
NCT05027217 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3421
Last updated 2023-06-06
Summary
Patients with acute severe health problems often need to be admitted to specialised hospital wards called Intensive Care Units (ICUs) where they can receive emergency treatment such as mechanical ventilation to support their breathing function via a machine, and sedative medications to reduce pain and anxiety associated with the severity of their condition.
Although these interventions and treatments are often necessary to support patients' vital functions, they also carry the risk of important side effects.
Sedative drugs use in particular, has a significant impact on short- and long-term outcomes.
Despite international guidelines to help clinicians in the use of these drugs, there appears to be large variability in their use around the world such as use of different types of drugs, variable doses or rate of continuous infusions, etc.
However, even with this known variable practice across the world, there are no large-scale international studies looking at the use of sedative drugs, pain-relief medications and drugs to control agitation and restlessness in ICUs.
Therefore, the investigators propose a multinational study to better understand how different ICUs use these drugs and if they follow the guidance published by expert clinicians. The investigators will collect data in more than 100 ICUs across the world and include more than 2000 adult patients admitted to ICU and needing mechanical breathing.
There are no active interventions on patients that are part of this research study and data collection from patients medical records is retrospective. All patients included will receive the standard of care as per their local intensive care unit.
Also, in a 2-arm sub-study, the investigators will collect retrospective data from medical records of patients admitted to ICU before and during the COVID-19 pandemic to explore how sedation, analgesia and delirium practice has changed during this exceptional timeframe.
Conditions
- Critical Illness
- Sedation Complication
- Intensive Care Unit Delirium
- Analgesia
- Covid19
Interventions
- OTHER
-
No intervention
No intervention. Arms are subdivided based on patients' diagnostic status on admission to ICU.
Sponsors & Collaborators
-
Mount Sinai Hospital, Canada
collaborator OTHER -
University of Oxford
lead OTHER
Principal Investigators
-
Sangeeta Mehta, Prof · Sinai Health, Toronto (Canada)
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-01-01
- Primary Completion
- 2023-05-15
- Completion
- 2023-05-30
Countries
- United Kingdom
Study Locations
More Related Trials
-
Development and Evaluation of Strategies to Improve Sedation Quality in InTensive Care
NCT01634451 ·Status: COMPLETED ·Phase: NA
-
Ketamine Versus Propofol as ICU Sedation
NCT06243822 ·Status: COMPLETED ·Phase: PHASE4
-
Effects of Combined Sevoflurane and Nitrous Oxide Inhalation - 14
NCT00000262 ·Status: COMPLETED ·Phase: NA
-
Volatile Sedation for Patients With the Acute Respiratory Distress Syndrome
NCT06014138 ·Status: RECRUITING ·Phase: PHASE2/PHASE3
-
Evaluation of Decision Capacity of ICU Patients Under Sedatives. A Prospective Observational Multicenter Study.
NCT04193540 ·Status: UNKNOWN
-
Analgesia-First Sedation in Trauma Patients
NCT05751863 ·Status: RECRUITING ·Phase: NA
-
Induction Agent Choice With Early Mortality and Prognostic Outcomes in Critically Ill Patients
NCT07222007 ·Status: RECRUITING
-
the Research of Analgesia and Sedation Effect of Remifentanil on ICU Short Operation
NCT02635802 ·Status: UNKNOWN ·Phase: PHASE4
-
Daily Sedative Interruption in Critically Ill Patients Being Managed With a Sedation Protocol.
NCT00675363 ·Status: COMPLETED ·Phase: NA
-
Propofol Sedation Study
NCT00597740 ·Status: COMPLETED
-
Effect of Sevoflurane, Propofol and Dexmedetomidine on Delirium & Neuroinflammation in Mechanically Ventilated Patients
NCT02394418 ·Status: WITHDRAWN ·Phase: PHASE4
-
Non-sedation Versus Sedation With a Daily Wake-up Trial in Critically Ill Patients Receiving Mechanical Ventilation
NCT01967680 ·Status: COMPLETED ·Phase: NA
-
The Effects of Ketamine on Respiratory Stimulation and Transpulmonary Pressures
NCT01969227 ·Status: COMPLETED ·Phase: NA
-
Ketamine Sedation in Mechanically Ventilated Patients
NCT00122759 ·Status: UNKNOWN ·Phase: NA
-
SedAting With Volatile Anesthetics Critically Ill COVID-19 Patients in ICU: Effects On Ventilatory Parameters And Survival
NCT04415060 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
AnaConDa Long Term Sedation Study
NCT01983800 ·Status: COMPLETED ·Phase: NA
-
Effect of Inhalation Sedation Compared With Propofol on the Sepsis-related Acute Respiratory Distress Syndrome Course
NCT04014218 ·Status: UNKNOWN ·Phase: PHASE4
-
Efficacy and Safety of Remifentanil for Mechanically Ventilated Patients in ICU
NCT05003570 ·Status: UNKNOWN ·Phase: PHASE3
-
Effects of Subanesthetic Isoflurane/Sevoflurane in 60% Oxygen on Clinical In-vitro Experimental Sepsis
NCT02185118 ·Status: UNKNOWN ·Phase: NA
-
Sevoflurane vs Nitrous Oxide Inhalation at Subanesthetic Concentrations - 11
NCT00000259 ·Status: COMPLETED ·Phase: NA
-
Inhalative Sedation in ICU With Sevoflurane Via Anaesthetic Conserving Device Compared to Propofol
NCT00586118 ·Status: COMPLETED
-
Inhaled Sedation in Critically Ill Patients
NCT07000526 ·Status: RECRUITING ·Phase: PHASE4
-
Ketamine Sedation in the ICU (KANINE) RCT
NCT06767358 ·Status: NOT_YET_RECRUITING ·Phase: PHASE3
-
A Comparison Between Propofol-Remifentanil and Midazolam-Remifentanil Sedation in the Intensive Care Unit
NCT01527903 ·Status: COMPLETED ·Phase: PHASE4
-
Comparison of an Inhaled Sedation Strategy to an Intravenous Sedation Strategy in Intensive Care Unit Patients Treated With Invasive Mechanical Ventilation
NCT04341350 ·Status: RECRUITING ·Phase: PHASE3