Clinical Trials Logo

Clinical Trial Summary

"In intensive care units, therapeutic paralysis has been a routine treatment method for many years in a select group of patients. Sufficient and appropriate sedation in patients undergoing therapeutic paralysis is crucial to prevent awareness and reduce the risk of excessive sedation. Both inadequate and excessive sedation levels can be highly detrimental to the patient. Clinical assessment may not always provide accurate information regarding sedation depth. Recently, the frequency and workload of therapeutic paralysis treatment in intensive care units have increased due to COVID-19 pneumonia. Therefore, the investigators believe that inadequate sedation may be common in these patients. Processed electroencephalogram parameters such as bispectral index or patient state index (PSI), routinely used in operating rooms and intensive care units, are commonly used to indicate sedation depth. In this study, the investigators aimed to determine sedation levels in patients during paralysis, assess the prevalence of inadequate or excessive sedation, and observe the doses of sedatives and analgesics used."


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06337877
Study type Observational
Source Tepecik Training and Research Hospital
Contact
Status Active, not recruiting
Phase
Start date October 1, 2023
Completion date April 24, 2024

See also
  Status Clinical Trial Phase
Completed NCT06033729 - Remifentanil Target Controlled Infusion Versus Standard of Care for Conscious Sedation During EBUS-TBNA N/A
Completed NCT04760249 - A Dedicated Sedation Team for Paediatric Procedural Sedation
Recruiting NCT05505279 - Ventilatory Effects of THRIVE During EBUS Phase 3
Recruiting NCT05267704 - Evaluating the Feasibility of VR for Pediatric Renal Biopsies N/A
Completed NCT06174168 - The Decisiveness of MFI-11 in Predicting Complications in Patients > 65 Years Who Underwent EBUS-TBNA Under Sedation
Recruiting NCT05969483 - Validation of a Processed EEG Device for Monitoring Sedation in PICU
Recruiting NCT06060626 - Optimization of Sedation Protocol for Endoscopic Procedures Using Impedance Ventilation Monitor. N/A
Recruiting NCT06014138 - Volatile Sedation for Patients With the Acute Respiratory Distress Syndrome Phase 2/Phase 3
Recruiting NCT05958537 - High Flow Nasal Oxygen Cannula in Transcatheter Aortic Valve Replacement: Complications and Biomarkers N/A
Recruiting NCT04801589 - Goal-Directed Sedation in Mechanically Ventilated Infants and Children Phase 3
Completed NCT05748626 - Anti-Snoring Appliances and Airway Manipulation in Patients Undergoing Anesthetic Sedation N/A
Recruiting NCT04727034 - Efficacy and Safety of Remimazolam Tosylate for Sedation in Gastroscopy N/A
Completed NCT06434428 - Comparison Between Intranasal vs Intravenous Dexmedetomidine for EEG Sedation of Children With Behavior Disorders.
Recruiting NCT05407870 - Efficacy and Safety of Etomidate Sedation in Gastric Endoscopic Submucosal Dissection N/A
Not yet recruiting NCT06459167 - Position Intervention to Reduce Hypoxemia in Sedation Patients N/A
Not yet recruiting NCT05423821 - Non-operating Room Anesthesia Experiences in Pediatric Magnetic Resonance Imaging Cases
Suspended NCT05399758 - Nociception Evaluated by the NOL® Index in Sedated Patients in the Intensive Care Unit
Completed NCT04410211 - Comparison Between Two Types of Sedation for Elective Upper Endoscopy Procedures N/A
Completed NCT04455776 - Safety Evaluation of Propofol Sedation for Magnetic Resonance Imaging in Pediatric Patients
Completed NCT05451121 - Effect of Sedation Strategy on Duration Mechanical Ventilation in Patient After Cardiac Surgery N/A