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The Effect of Thoracic Epidural Anesthesia With Different Block Level on Propofol Induction

NCT02135016 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2014-08-29

Study results available
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Summary

It is a prospective, randomized, placebo-controlled study to investigate the effect of TEA with different block level on propofol concentration during general anesthesia induction.

Conditions

  • Target Controlled Infusion (TCI)
  • Thoracic Epidural Anesthesia
  • Block Level
  • Gastrointestinal Surgery

Interventions

DRUG

1% lidocaine

epidural anesthesia with 1% lidocaine 10ml before propofol TCI

DRUG

2% lidocaine

epidural anesthesia with 2% lidocaine 5ml before propofol TCI

DRUG

0.9% normal saline

epidural anesthesia with 0.9% normal saline 5ml before propofol TCI

Sponsors & Collaborators

  • First Hospital of China Medical University

    lead OTHER

Principal Investigators

  • Jun Wang, professor · Dept. of Anesthesiology, First Affiliated Hospital of China Medical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-04-30
Primary Completion
2014-07-31
Completion
2014-07-31

Countries

  • China

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 NCT02135016 on ClinicalTrials.gov