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Effect of Flumazenil on Postoperative Memory Retention Time after General Anesthesia with Remimazolam: A Randomized Controlled Trial

Effect of Flumazenil on Postoperative Memory Retention Time after General Anesthesia with Remimazolam: A Randomized Controlled Trial - Effect of Flumazenil on Postoperative Memory Retention Time after General Anesthesia with Remimazolam: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052659
Enrollment
44
Registered
2023-11-01
Start date
2023-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients scheduled for breast surgery under general anesthesia

Interventions

Flumazenil group after general anesthesia No flumazenil administered after general anesthesia group

Sponsors

Kyushu University Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria will be eligible 1. the patient has given written consent of his/her own free will 2. age between 20 and 65 years old at the time of consent 3. scheduled to undergo breast surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: Patients will be excluded from the study if any of the following apply 1) Patients with a history of hypersensitivity to remimazolam or flumazenil 2. patients with acute angle closure glaucoma, myasthenia gravis, epilepsy patients who have been receiving benzodiazepines for a long period of time, or have a history of serious complications or illnesses that would make them inappropriate for participation in this study Patients who are deemed inappropriate for inclusion in the study by the investigator. 4. (4) Patients with ASA physical status of IV or higher, shock, or coma (5) Patients with cognitive impairment 5. patients with cognitive impairment

Design outcomes

Primary

MeasureTime frame
Time for 80% of patients or all patients in each group to be able to memorize. If the patient had no memory of Illustration A 1 hour after leaving the operating room, one more poster (Illustration B) was shown, and 2 hours after leaving the operating room, the patient's memory of Illustration B was checked. If the patient has no memory of Illustration B, one more poster (Illustration C) is shown, and 3 hours after leaving the operating room, the patient's memory of Illustration C is checked. If the patient remembers Illustration C, the evaluation is terminated at that point.

Secondary

MeasureTime frame
(1) Percentage of patients whose memory of the poster shown after awakening from anesthesia could be confirmed 1 hour after leaving the operating room. (2) Dosage and frequency of analgesic use from the time of return to the ward to 3 hours after surgery (3) Dosage and frequency of antiemetic use from the time of return to the ward to 3 hours after surgery

Countries

Japan

Contacts

Public ContactKazuhiro Shirozu

Kyushu University Hospital Operating room

shirozu.kazuhiro.334@m.kyushu-u.ac.jp092-642-5714

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026