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Compare the Side Effects and Difference Awake Level of Three TCI Propofol Formula in TVOR Patients

NCT00760253 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 118

Last updated 2009-12-15

No results posted yet for this study

Summary

This study is to find the fewer side effects formula of anesthesia for TVOR patients, to compare the BIS level during emergence and to find the correlation between BIS and transcutaneous carbon dioxide concentration.

Conditions

  • Bispectral Index
  • Transcutaneous Carbon Dioxide
  • PONV
  • Blood Pressure
  • Heart Rate

Sponsors & Collaborators

  • National Taiwan University Hospital

    lead OTHER

Principal Investigators

  • Chuen-shin Jeng, MD, MS · Visiting staff

Eligibility

Min Age
25 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-09-30
Primary Completion
2008-10-31
Completion
2008-12-31

Countries

  • Taiwan

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 NCT00760253 on ClinicalTrials.gov