Effectiveness of the NeuroSENSE for Monitoring the Hypnotic Depth of Anesthesia

• Status: Completed
• Trial end date: 2016-10-01
• Target enrollment: 0
• Participant gender: All

Summary

The objective of this clinical study is to investigate whether the NeuroSENSE is an adequate monitor of hypnotic depth-of-anesthesia (DOA). Therefore, this study will investigate whether the information provided by the NeuroSENSE Monitor can help in assessing the hypnotic effect of anesthetics in adult patients undergoing general anesthesia.

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: NeuroWave Systems Inc.
• Collaborators: Fraser Health; U.S. Army Medical Research Acquisition Activity
• Treatments: Anesthetics; Desflurane; Hypnotics and Sedatives; Isoflurane; Propofol

Criteria

Inclusion Criteria:

• age 18-75 years

• ASA (American Society of Anesthesiologist) physical status I, II, or III

• ability to read and understand the informed consent form

• undergoing anesthesia procedure requiring intubation

• scheduled to undergo either open or laparoscopic abdominal surgical procedures (e.g. colectomy, hysterectomy, radical retropubic prostatectomy, nephrectomy, pancreatectomy, etc.), breast surgery including reduction, reconstruction and mastectomies, or orthopedic surgeries under general anesthesia, expected to last at least 1 hour.

Exclusion Criteria:

• history of major head injury (possible abnormal EEG)

• acquired scalp or skull abnormalities (e.g. psoriasis, eczema, angioma, scar tissue, burr holes, cranial implants)

• evidence of recent trauma or active neurological disorder, stroke, seizure disorder, intellectual disability, dementia or diagnosis of Alzheimer's disease

• major antipsychotic medications taken within last 7 days (eg. Lithium, risperidone, olanzapine)

• known history of alcohol or drug abuse within last 30 days

• body mass index (weight in kilograms divided by square of height in meters) > 40.0 kg/m2

• uncontrolled hypertension with blood pressure recorded prior to surgery (systolic blood pressure > 200 mmHg or diastolic blood pressure > 110 mmHg)

• systolic blood pressure < 90 mmHg, recorded prior to surgery

• heart rate (HR) < 45 beats/min, recorded prior to surgery

• insulin-dependent diabetes mellitus

• pregnancy

• any serious medical condition that would interfere with cardiovascular response assessment or study results interpretation