Clinical trial

The Impact of Administration of Flumazenil on the Emergence Delirium in Patients Anesthetized With Remimazolam: a Prospective Randomized Single-blind Study

Name
2022GR0520
Description
Flumazenil rapidly antagonizes benzodiazepines (BZDs); it may induce agitation, seizure, or delirium, especially when applied to patients who have taken BZDs for a long time. On the contrary, it may help patients regain consciousness in a stable and calm state by appropriately reversing the central nervous system depressant effects of BZDs. In this study, we aim to investigate the impact of flumazenil on the emergence delirium in patients anesthetized with remimazolam, the short-acting BZD drug.
Trial arms
Trial start
2023-03-05
Estimated PCD
2023-08-11
Trial end
2023-08-11
Status
Completed
Phase
Early phase I
Treatment
Flumazenil
After cessation of remimazolam infusion, flumazenil 0.2 mg is administered intravenously over 15 seconds. If consciousness is not adequately restored within 3-5 minutes, a second dose of 0.1 mg intravenously over 15 seconds is administered. If necessary, 0.1 mg may be administered repeatedly at 3-5 minute intervals, and the maximum dose of 1 mg should not be exceeded.
Arms:
Flumazenil group
Size
68
Primary endpoint
Incidence of emergence delirium
From emergence to postanesthesia care unit (PACU) discharge (Immediately after extubation, 15 min after PACU admission, PACU discharge) [within 2 hrs after surgery]
Eligibility criteria
Inclusion Criteria: * Adult patients aged 19 years or older undergoing surgery under general anesthesia Exclusion Criteria: * Peripheral nerve block or Neuraxial block * Uncontrolled hypertension (HTN) (systolic blood pressure (SBP) ≥180 mmHg) * Uncontrolled diabetes mellitus (DM) (HbA1c ≥9.0%) * Hepatic dysfunction (Total bilirubin ≥3.0 mg/mL or Liver enzyme ≥Upper normal limit x 2.5) * Renal dysfunction (Estimated glomerular filtration rate (eGFR) \<30 ml/min/1.73m2 or Dialysis) * Moderate or severe chronic obstructive pulmonary disease or Respiratory failure * Emergency * Hepatectomy or Liver transplantation * Intraoperative cardiopulmonary bypass (CPB) or extracorporeal membrane oxygenation (ECMO) use * Head trauma, Increased intracranial pressure, Craniotomy * Chronic use of benzodiazepines (BZDs) * Anxiety, Alcohol/Drug dependence, Addiction to tricyclic antidepressants (TCAs) * Allergic reaction to BZDs, flumazenil, or other drugs used in general anesthesia * Severe allergy or Anaphylaxis history * Lactose-related genetic disorders * Myasthenia gravis or Myasthenia gravis syndrome * Myocardial infarction or Cerebrovascular events within 6 months * Symptomatic coronary artery disease * Organic brain disease * Cognitive impairment (Inability to understand informed consent)
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'TRIPLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 68, 'type': 'ACTUAL'}}
Updated at
2023-09-06

1 organization

1 product

2 indications

Product
Flumazenil
Indication
Anesthesia
Indication
General