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Transesophageal Echocardiographic Evaluation of the Effect of Dexmedetomidine Infusion as an Adjuvant to General Anesthesia on the Cardiac Function

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Yonsei University

Status

Completed

Conditions

Anesthesia

Treatments

Drug: Dexmedetomidine, Transesophageal echocardiography(TEE)
Drug: Saline will be infused for 60 minutes at the same rates as dexmedetomidine group.

Study type

Interventional

Funder types

Other

Identifiers

NCT02300649
4-2014-0574

Details and patient eligibility

About

Dexmedetomidine is a selective alpha-2 adrenergic agonist that can be considered as an adjuvant to propofol or inhalational anesthetics. Dexmedetomidine mediate its cardiovascular effect through activation of receptors in central and peripheral nervous system. The classic cardiovascular response of dexmedetomidine is the biphasic with initial short-term increase in blood pressure followed by long-lasting decrease in BP and HR. There were several reports about these hemodynamic changes of dexmedetomidine, but not the evaluation of direct effects on cardiac function. The purpose of this study is to evaluate the effects of dexmedetomidine as an anesthetic adjuvant on cardiac function by using the transesophageal echocardiography.

Enrollment

30 patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Above 20 years of age.
  2. American Society of Anesthesiologists (ASA) Physical Status I, II, III.
  3. general anesthesia

Exclusion criteria

  1. severe functional liver or kidney disease
  2. diagnosed HF ( NYHA class >3)
  3. arrhythmia or received treatment with antiarrythmic drug .
  4. severe bradycardia (HR < 45 bpm) and AV block
  5. pathologic esophageal lesion (esophageal stricture or varix )
  6. pregnancy

Trial design

30 participants in 2 patient groups, including a placebo group

Dexmedetomidine group
Experimental group
Description:
Dexmedetomidine will be infused at a rate of 6 mcg/kg/hr for 10 minutes; resulting in a loading dose of 1 mcg/kg, followed by an infusion of 0.5 μg/kg/hr for 50 minutes.
Treatment:
Drug: Dexmedetomidine, Transesophageal echocardiography(TEE)
Control group
Placebo Comparator group
Description:
Saline will be infused at a rate of 6 mcg/kg/hr for 10 minutes; resulting in a loading dose of 1 mcg/kg, followed by an infusion of 0.5 μg/kg/hr for 50 minutes.
Treatment:
Drug: Saline will be infused for 60 minutes at the same rates as dexmedetomidine group.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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