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Dexmedetomidine on Segmental EEG Power Spectra

Conditions
EEG Power Spectra
Anesthesia
Registration Number
NCT03515876
Lead Sponsor
Zhiyi Zuo
Brief Summary

To compare the EEG power spectra activity during propofol-based anesthesia in the presence or absence of dexmedetomidine in patients undergoing hysteroscopic examination and surgery to determine whether the addition of dexmedetomidine will induce better sleep-like anesthesia status.

Detailed Description

Three groups of patients undergoing hysteroscopic examination and surgery will be studied: 1) control group, patients will receive propofol intravenous infusion to provide anesthesia; 2) dexmedetomidine 0.5 microgram/kg group. This dexmedetomidine dose is infused within 10 min and then the use of propofol for anesthesia; and 3) dexmedetomidine 1 microgram/kg group. This dexmedetomidine dose is infused within 10 min and then the use of propofol for anesthesia.

Each group will have 20 patients.

General conditions including blood pressure, respiration, and heart rates will be recorded.

EEG power spectra activity will be recorded no-invasively by a Narcotrend EEG monitor.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
60
Inclusion Criteria
  • American Society of Anesthesiologists Physical status I to II grade.
  • body mass index 18 to 25 kg/m2
  • no vision or hearing impairment
  • will receive general anesthesia
Exclusion Criteria
  • with psychological or mental diseases
  • with neurological diseases
  • treating with steroids or with alcohol dependence.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
EEG power spectraFrom prior to anesthesia to 10 min after anesthesia.

EEG power spectra monitored no-invasively by Narcotrend

Secondary Outcome Measures
NameTimeMethod
Blood pressureFrom prior to anesthesia to 10 min after anesthesia.

Blood pressure monitored no-invasively

RespirationFrom prior to anesthesia to 10 min after anesthesia.

Monitored no-invasively

Heart ratesFrom prior to anesthesia to 10 min after anesthesia.

Monitored no-invasively

Trial Locations

Locations (1)

Sun Yat-Sen Memorial Hospital

🇨🇳

Guangzhou, Guangdong, China

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