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The Effect of Bispectral Index Monitoring on Recovery From Deep Sedation

NCT04190082 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2023-02-15

No results posted yet for this study

Summary

The purpose of this study was to compare BIS (bispectral index) monitoring and clinical sedation scale assessment on the recovery time and propofol usage from deep propofol sedation in children with cerebral palsy who received botulinum toxin injection.

Conditions

  • Cerebral Palsy

Sponsors & Collaborators

  • Yeungnam University College of Medicine

    lead OTHER

Principal Investigators

  • Sung Mee Jung, MD,PhD · Yeungnam University Hospital

Eligibility

Min Age
3 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-01
Primary Completion
2022-12-09
Completion
2022-12-09

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04190082 on ClinicalTrials.gov