Effects of Dexmedetomidine on Cardiac Electrophysiology in Patients Under General Anesthesia During Perioperative Period

Sponsor
Yangzhou University (Other)
Overall Status
Completed
CT.gov ID
NCT04577430
Collaborator
(none)
81
1
4
18.2
4.4

Study Details

Study Description

Brief Summary

Perioperative stress may increase the incidence of adverse events in the cardiovascular system and lead to poor prognosis. Dexmedetomidine is a highly selective α2 adrenergic receptor agonist, which can inhibit stress response and reduce hemodynamic fluctuations. In different usage plans, dexmedetomidine can have different effects on hemodynamics, myocardial electrical activity, cardiac function. The main purpose was to observe its effects on myocardial electrophysiology and cardiac function during perioperative period. The secondary purpose was to explore the optimal dose of dexmedetomidine that has the least adverse effects on perioperative electrocardia action and cardiac function

Study Design

Study Type:
Interventional
Actual Enrollment :
81 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Effects of Dexmedetomidine on Cardiac Electrophysiology in Patients Under General Anesthesia During Perioperative Period
Actual Study Start Date :
Sep 8, 2019
Actual Primary Completion Date :
Feb 1, 2021
Actual Study Completion Date :
Mar 16, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Loading dose with 0.5 μg/kg, maintenance dose with 0.5 μg/kg

10 min before induction of anesthesia,the loading dose of dexmedetomidine is 0.5 μg/kg, and completed in 10 minutes. The maintenance dose is 0.5 μg/kg per hour during the operation until 0.5 h before the operation finished.

Drug: Dexmedetomidine
The loading dose with 0.5 μg/kg, maintenance dose with 0.5 μg/kg of Dexmedetomidine is used to observe the effect on the electrophysiology of the patients' hearts

Experimental: Loading dose with 1 μg/kg, maintenance dose with 0.5 μg/kg

10 min before induction of anesthesia,the loading dose of dexmedetomidine is 1 μg/kg, and completed in 10 minutes. The maintenance dose is 0.5 μg/kg per hour during the operation until 0.5 h before the surgery finished.

Drug: Dexmedetomidine
The loading dose with 1 μg/kg, maintenance dose with 0.5 μg/kg of Dexmedetomidine is used to observe the effect on the electrophysiology of the patients' hearts

Experimental: Loading dose with 1 μg/kg, maintenance dose with 1 μg/kg

10 min before induction of anesthesia,the loading dose of dexmedetomidine is 1 μg/kg, and completed in 10 minutes. The maintenance dose is 1 μg/kg per hour during the operation until 0.5 h before the surgery finished.

Drug: Dexmedetomidine
The loading dose with 1 μg/kg, maintenance dose with 1 μg/kg of Dexmedetomidine is used to observe the effect on the electrophysiology of the patients' hearts

Placebo Comparator: Normal saline

Drug: Normal saline
Normal saline is used to observe the effect on the electrophysiology of the patients' hearts

Outcome Measures

Primary Outcome Measures

  1. The length of PR,QRS,QTc,QT and Tp-e intervals and the level of iCEB [during surgery to 1 month after the surgery]

    All the outcomes above should be measured at the time preparing to pump a loading dose,the time after the loading dose finished,at the end of surgery,1h after the surgery finished,24 h after the surgery finished,48 h after the surgery finished,72 h after the surgery finished,1 month after the surgery finished

Secondary Outcome Measures

  1. The level of Na+,iCa2+ [perioperative]

    All the outcomes above should be measured at the time preparing to pump a loading dose,the time after the loading dose finished,1h after the beginning of the surgery,the end of surgery,1h after the surgery finished

  2. The level of cardiac circulation efficiency [Perioperative]

    All the outcomes above should be measured at the time preparing to pump a loading dose,the time after the loading dose finished,1h after the beginning of the surgery,the end of surgery,1h after the surgery finished

  3. The level of maximum pressure gradient [Perioperative]

    the time preparing to pump a loading dose,the time after the loading dose finished,the beginning of surgery, 30min after the beginning of surgery,1h after the beginning of the surgery,the end of surgery,1h after the surgery finished

  4. The level of heart rate [Perioperative]

    the time preparing to pump a loading dose,the time after the loading dose finished,the beginning of surgery, 30min after the beginning of surgery,1h after the beginning of the surgery,the end of surgery,1h after the surgery finished

  5. The level of mean arterial blood pressure [Perioperative]

  6. The level of systemic vascular resistance [Perioperative]

    the time preparing to pump a loading dose,the time after the loading dose finished,the beginning of surgery, 30min after the beginning of surgery,1h after the beginning of the surgery,the end of surgery,1h after the surgery finished

  7. The time of eyes opening from surgery ending,the whole surgery,anesthesia [intraoperative]

  8. The dosage of propofol and remifentanil [intraoperative]

  9. Total fluid intake from entering the operating room to exiting the PACU [Perioperative]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Ages ranged from 18 to 65

  • ASA I~II

  • patients undergoing elective general anesthesia

  • the surgery time for 1~3 h

Exclusion Criteria:
  • Preoperative ECG abnormalities, including QTc ≥440 ms (male), 460ms (female)

  • abnormal cardiac conduction, prolonged QT syndrome

  • heart disease history, such as pacemaker implantation, unstable angina, congestive heart failure, Heart valve disease

  • antiarrhythmic drugs (β-receptor blockers, calcium channel blockers, tricyclic antidepressants, etc.) that can prolong the QT interval taken within one week before surgery

  • coronary heart disease, non-sinus Heart rhythm, bradycardia, tachycardia, other arrhythmia, etc

  • intraoperative HR≤45 beats/min and need drugs to increase heart rate

  • previous allergy to dexmedetomidine

  • preoperative electrolyte abnormalities

  • emergency surgery, neurological or mental disorders , Liver and kidney dysfunction

  • patients who use analgesic pumps after surgery

  • refusal of patients

Contacts and Locations

Locations

Site City State Country Postal Code
1 the Affiliated Hospital of Yangzhou University, Yangzhou University Yangzhou Jiangsu China 225012

Sponsors and Collaborators

  • Yangzhou University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Zhuan Zhang, Principal Investigator, Yangzhou University
ClinicalTrials.gov Identifier:
NCT04577430
Other Study ID Numbers:
  • 20200915
First Posted:
Oct 6, 2020
Last Update Posted:
Aug 31, 2021
Last Verified:
Mar 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 31, 2021