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Japanese

Feb. 06, 2025

April. 09, 2026

jRCTs021240059

A study of the Rapid Sequence Awakeness method by reversing remimazolam with flumazenil in pediatric anesthesia, A randomized controlled study

Remimazolam and flumazenil for Rapid Sequence Awakeness method in pediatric anesthesia

Yakushiji Tatsumi

Fukushima Medical University Hospital

1 Hikarigaoka, Fukushima City, Fukushima Prefecture

+81-24-547-1342

tatsumiy@fmu.ac.jp

Yakushji Tatsumi

Fukushima Medical University Hospital

1 Hikarigaoka, Fukushima City, Fukushima Prefecture

+81-24-547-1342

masui@fmu.ac.jp

Recruiting

Feb. 06, 2025

Feb. 27, 2025
108

Interventional

randomized controlled trial

open(masking not used)

active control

parallel assignment

other

Patients scheduled for surgery under general anesthesia who meet the following criteria.
1) Patients 1-6 years of age at the time of consent.
2) Patients with an American Society of Anesthesiologists physical status (ASA-PS) of 1-2 at the preoperative visit.
3) Patients scheduled to have their airway secured by oral tracheal intubation.
4) Patients scheduled for extubation in the operating room.
5) Patients who have been fully informed about the study and have provided written informed consent from a surrogate.

1) Patients scheduled to undergo craniotomy
2) Patients whose scheduled operation time is less than 20 minutes but longer than 4 hours
3) Patients who are expected to bleed heavily (more than 15% of circulating blood volume) during surgery
4) Patients who are expected to have difficulty with mask ventilation, intubation, but extubation
5) At risk of vomiting or aspiration during the perioperative period
6) Patients with a history of severe allergy to benzodiazepines, flumazenil citrate, remifentanil hydrochloride, fentanyl citrate, rocuronium bromide, or sugammadex sodium
7) Patients who have been taking benzodiazepines regularly before surgery or have a history of tolerance to benzodiazepines
8) Patients with a history of epilepsy
9) Patients with a history of glaucoma
10) Other patients deemed inappropriate by the principal investigator or subinvestigator

1age 0month old over
6age 12month old under

Both

Diseases for which scheduled surgery is performed under general anesthesia

Awake group: Maintain anesthesia with sevoflurane, and extubate after confirming the patient's awakening.
RSA group: Switch from sevoflurane to remimazolam as maintenance drug before the end of surgery, and administer flumazenil and extubate the patient after confirming spontaneous respiration

Incidence of EA/ED up to 15 minutes after awakening and extubating

PAEDs score on admission to the PICU and at each time point (*) after admission to the PICU
Percentage of EAs/EDs on admission to the PICU and at each time point (*) after admission to the PICU
Percentage of PRAEs in the operating room
Percentage of PRAEs occurring up to 2 hours after PICU admission
Percentage of cases requiring airway/respiratory intervention within 2 hours of PICU admission
Percentage of resuscitations within 2 hours of PICU admission
Time from end of surgical procedure to patient leaving the operating room
FLACCs score after extubation
FLACCs score on admission to PICU and at each assessment time point (*)
Subjective assessment by anesthesiologist of quality of emergence and extubation from general anesthesia.
*Evaluation time points are defined as at the time of admission to the PICU + 10 minutes and 30 minutes +/- 10 minutes, 60 minutes +/- 10 minutes, and 120 minutes +/- 10 minutes after admission to the PICU.

Fukushima Medical University Certified Review Board
1 Hikariga-oka, Fukushima City, Fukushima, 960-1295 Japan, Hukushima

+81-24-547-1825

fmucrb@fmu.ac.jp
Approval

Jan. 24, 2025

No

none

History of Changes

No Publication date
3 April. 09, 2026 (this page) Changes
2 Sept. 17, 2025 Detail Changes
1 Feb. 06, 2025 Detail