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The EC50 of Remifentanil Blunting Hemodynamic Response to Double Lumen Tube Intubation

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Seoul National University

Status

Completed

Conditions

Hemodynamic Responses During Tracheal Intubation

Treatments

Drug: Remifentanil

Study type

Interventional

Funder types

Other

Identifiers

NCT01542099
JHBahk_DLT_remi

Details and patient eligibility

About

The purpose of this study is to evaluate the effect site concentration of remifentanil blunting hemodynamic changes to tracheal intubation of single or double lumen tubes.

Enrollment

80 patients

Sex

All

Ages

20 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing thoracic surgery that require one lung ventilation

Exclusion criteria

  • patient who does not agree with this study
  • BMI < 16.0 or BMI > 30
  • cardiovascular disease, pulmonary disease, renal disease
  • alcoholic abuser or drug abuser
  • patient who takes any drug to influence cardiovascular system or sympathetic nervous system
  • any use of local anesthetics or drugs to influence cardiovascular system during tracheal intubation

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Single lumen tube
Active Comparator group
Description:
Single lumen tube intubation during remifentanil infusion
Treatment:
Drug: Remifentanil
Drug: Remifentanil
Double lumen tube
Active Comparator group
Description:
Double lumen tube intubation during remifentanil infusion
Treatment:
Drug: Remifentanil
Drug: Remifentanil

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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