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Completed NCT03575169

The Use of Bispectral Index Monitoring to Assess Depth of Sedation in Patients With Traumatic Brain Injury

Conditions: Traumatic Brain Injury

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 26
Sponsor: University of Aberdeen

Location: Intensive Care Unit, Aberdeen Royal Infirmary Aberdeen

Summary

An observational study to assess the BIS reported level of sedation of patients with traumatic brain injury in the ICU.

Eligibility Criteria

Inclusion Criteria: * Adults (over 18) * Diagnosis of traumatic brain injury * Expected to survive * Expected to require greater than 24 hours of sedation and mechanical ventilation Exclusion Criteria: * Brain injury thought to be unsurvivable by ICU clinical team * Frontal decompressive craniectomy * Use of ketamine infusion at recruitment or planned use within 24 hours * Fractured frontal bone or severe overlying soft tissue injury * Simple extradural haemorrhage with no other obvious intracranial injury * Pregnant patient

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT03575169). StuddyBuddy aggregates publicly available trial information.