Clinical Trials Logo

Clinical Trial Summary

ConsCIOUS-2 is a multi-site study exploring the cognitive state of the Isolated Forearm Test (IFT) responder while under anesthetic.


Clinical Trial Description

500 participants between the ages of 18-40 who will be undergoing surgery requiring general anesthetic will be recruited for this study. This study will use the Isolated Forearm Test (IFT) to identify patients at risk of anesthesia awareness. In the IFT, induction of anesthesia is followed by inflation of a cuff on the dominant arm before neuromuscular blockade (paralysis) is induced. The cuff prevents paralysis of the hand allowing the patient to communicate to an observer through predefined hand movements, typically following a command like: "Mrs. Jones, if you can hear me, squeeze my hand". Participants will thus be asked to follow a series of commands intraoperatively to assess awareness. Routinely recorded clinical data will be collected to frame the observations about IFT responsiveness, and non-invasive EEG data will also be collected to provide information about the "brain state" of the patients. Patient reported confusion and objectively measured confusion using the Nurse Based Delirium Screening Tool (NuDesc) will be collected post operatively. Finally, participants will be contacted 24 hours and 7 days following their operation to complete an anesthesia satisfaction questionnaire. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03503357
Study type Interventional
Source University of Wisconsin, Madison
Contact
Status Completed
Phase N/A
Start date April 4, 2018
Completion date December 23, 2019

See also
  Status Clinical Trial Phase
Completed NCT05346588 - THRIVE Feasibility Trial Phase 3
Recruiting NCT05991453 - Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial N/A
Completed NCT05656703 - Anesthesia Depth Increases Delirium Incidence N/A
Recruiting NCT03773588 - Entropy and Surgical Pleth Index Guided Closed Loop Target Controlled Infusion Total Intravenous Anesthesia With Propofol N/A
Active, not recruiting NCT06337877 - Assessment of Sedation Depth in ARDS Patients Undergoing Therapeutic Paralysis
Completed NCT03438734 - Comparison of Low Versus Normal Flow Anesthesia on Cerebral Oxygenation and Bispectral Index in Morbidly Obese Patients N/A
Not yet recruiting NCT06427785 - The Effect of Wavelet Index in Monitoring the Sedation Depth of Remimazolam Besylate
Completed NCT06316622 - Examination of The Relationshıp Between Body Mass Index And The Skin-Epidural Space Distance N/A
Recruiting NCT06323616 - The Effect of Anesthesia Depth Monitoring on Emergence Delirium in Pediatrics N/A
Recruiting NCT03476213 - Manual Versus Targer-controll Infusion in Reduction of Awareness and Dreaming N/A
Recruiting NCT04009018 - Adaptation of Perioperative Satisfaction Scale in Regional Anesthesia and Investigation of Its Psychometric Properties N/A
Suspended NCT03498391 - A Study of Human Multi-Sensory Integration Phase 2
Completed NCT03521414 - Glasgow Coma Scales and General Anesthesia N/A
Completed NCT03134651 - Preoperative Anxiety at Oocyte Retrieval N/A
Active, not recruiting NCT04826146 - Pediatric Validation of CONOX Monitor During Surgery
Recruiting NCT04788732 - Heart Rate Variability to Quantify General Anesthesia Depth
Recruiting NCT05193747 - The Depth of Paediatric Anaesthesia: Observational Trial
Completed NCT03807297 - TIVA vs Inhalational Mode of Anaesthesia Phase 2
Completed NCT04813952 - The Effect of Minimal Flow Sevoflurane Anesthesia N/A
Not yet recruiting NCT05254704 - Validation of the French Version of the TEX-Q Questionnaire.