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UnknownNCT03515876

Dexmedetomidine on Segmental EEG Power Spectra

The Effects of Dexmedetomidine on Segmental EEG Power Spectra Activity Under Propofol-based Anesthesia

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Zhiyi Zuo · Academic / Other
Sex
Female
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2018-04-19
Primary completion
2019-06-01
Completion
2019-07-01
First posted
2018-05-04
Last updated
2019-04-09

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03515876. Inclusion in this directory is not an endorsement.