Evaluation of the efficacy of dexmedetomidine as an anesthetic and effects of spinal cord monitoring

Phase 1

• Conditions: Spinal cord tumors, spinal disorders

• Registration Number: JPRN-UMIN000009044
• Lead Sponsor: iigata University Medical and Dental Hospital, Anesthesiology

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-10-05
• Study Completion: 2013-04-01
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

Not provided

Exclusion Criteria

1.Patients who are or may be pregnant. 2.Patients undergoing blood purification therapy. 3. Patients with cardiovascular disorders. 4.Patients with reduced cardiac function. 5.Patients with a reduced circulating blood volume. 6.Patients with liver dysfunction. 7.Patients with kidney dysfunction. 8.Old patients (75 years or above). 9.Patients judged to be inappropriate.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To evaluate the depth of anesthesia by BIS monitoring to validate the hypothesis that dexmedetomidine is effective as a general anesthetic.

Secondary Outcome Measures

Name	Time	Method
To measure the amplitude and latency of the waveform obtained by spinal cord monitoring under general anesthesia using dexmedetomidine, and to evaluate its clinical advantages and safety.