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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05201300
Other study ID # AJIRB-MED-INT-21-651
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 2, 2022
Est. completion date January 18, 2023

Study information

Verified date July 2023
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Remimazolam is a recently developed ultra-short agonist acting at the benzodiazepine binding site of the gamma-aminobutyric acid (GABA)A receptor. Remimazolam has a combination of the hemodynamic stability of benzodiazepines and the advantages of propofol, such as rapid onset, short duration of action, and improved controllability. A recent study showed that the efficacy of two induction doses of remimazolam (6 and 12 mg/kg/h) as a sedative for general anesthesia was not inferior to propofol (2.0-2.5 mg/kg), and hemodynamically more stable. On the other hand, a study on the emergence time and quality between propofol and remimazolam showed inconsistent results. The purpose of this study is to compare remimazolam to propofol on the intraoperative hemodynamic changes and recovery profiles, when used in combination with remifentanil in elderly patients undergoing general anesthesia.


Recruitment information / eligibility

Status Completed
Enrollment 69
Est. completion date January 18, 2023
Est. primary completion date November 25, 2022
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria: - ASA I, II patients over 65 years old undergoing general anesthesia Exclusion Criteria: - cardiac surgery - neurosurgery - liver surgery - uncontrolled hypertension - bronchial asthma - body mass index = 30 kg/m2 - severe heart, liver, kidney disease

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Remimazolam Besylate 6 mg/kg/hr
Patients will receive remimazolam at 6 mg/kg/hr by continuous infusion until loss of consciousness.
Remimazolam Besylate 12 mg/kg/hr
Patients will receive remimazolam at 12 mg/kg/hr by continuous infusion until loss of consciousness.
Propofol
Patients will receive propofol at a target controlled infusion 4 µg/ml until loss of consciousness.

Locations

Country Name City State
Korea, Republic of Ajou University Hospital Suwon Gyeonggi-do

Sponsors (1)

Lead Sponsor Collaborator
Ajou University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary difference in the decreased mean arterial pressure difference between baseline mean arterial pressure and lowest mean arterial pressure from the start of anesthetics (propofol or remimazolam) injection to the 5 minutes after extubation
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