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The comparison of electroencephalogram changes by different sedatives in intensive care unit patients

The comparison of electroencephalogram changes by different sedatives in intensive care unit patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16008882
Enrollment
Unknown
Registered
2016-07-22
Start date
2016-08-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

unlimited

Interventions

Dex group:receive dexmedetomidine sedation
Pro group:receive propofol sedation

Sponsors

the First Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 18 or over 18 years old, male or female; conscious;receiving assisted ventilation and requiring sedative and analgesic medication; expected to stay in ICU for more than 24 hours.

Exclusion criteria

Exclusion criteria: Patient is pregnant or lactating;Proven or suspected acute primary brain lesion such as traumatic brain injury, cerebrovascular accident, or hypoxic-ischemic encephalopathy; spinal cord injury or myasthenia gravis; Mean arterial blood pressure (MAP) that is less than 50 mmHg despite adequate resuscitation and vasopressor therapy; Heart rate less than 55 beats per minute without being treated with a beta-blocker or a high grade atrio-ventricular block in the absence of a functioning pacemaker; subjects with portal hypertension complicated by gastrointestinal bleeding, acute liver failure or Hepatic encephalopathy; A history of schizophrenia, epilepsy or Parkinsonian syndrome; patients who can not finish the evaluation of pain, sedation or delirium due to severe dementia, coma or end-stage disease, etc.

Design outcomes

Primary

MeasureTime frame
amplitude-integrated electroencephalogram (aEEG);spectral entropy;relative spectral power;spectral edge frequency;

Secondary

MeasureTime frame
RASS score;mechanical ventilating duration;length of ICU stay;proportion of patients with delirium;heart rate;blood pressure;cumulative dose of rescue sedative agent;NSE;s100ß;CPOT score;

Countries

China

Contacts

Public ContactChen Minying

the First Affiliated Hospital of Sun Yat-sen University

chmy1969@hotmail.com+86 13925019136

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026