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Study on the interaction between remimazolam and inhaled anesthetics (sevoflurane)

Study on the interaction between remimazolam and inhaled anesthetics (sevoflurane)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1041230104
Enrollment
100
Registered
2023-11-10
Start date
2023-11-10
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

Patient undergoing general anesthesia and i-gel insertion

Interventions

Remimazolam and sevoflurane are administered at assigned doses during general anesthesia.

Sponsors

Kobayashi Kensuke
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. patients who are between 40 and 60 years of age at the time of consent 2. patients scheduled for i-gel insertion for non-emergency (scheduled or temporary) surgery 3. patients with ASA (American Society of Anesthesiologists) Class I or II status 4. patients who have given their consent to this study by signing the consent form

Exclusion criteria

Exclusion criteria: 1. those who are expected to have difficulty in intubation (e.g., with impaired opening, Mallampati Grade III or IV, etc.) 2. 2. patients undergoing surgery requiring intubation 3. patients with symptoms of airway infection 4. benzodiazepines or benzodiazepines 4. patients with a history of hypersensitivity to benzodiazepines or flumazenil 5. patients who should avoid sevoflurane (e.g., history of malignant hyperthermia or family history of malignant hyperthermia) 6. patients with a history of hypersensitivity to rocuronium 7. severely obese (BMI > 35) Pregnant patients 9. nursing mothers and postpartum mothers 10. patients with the possibility of aspiration 11.Patients with a history of hypersensitivity to remimazolam 12.Patients with a history of glaucoma 13.Patients who regularly use benzodiazepines 14.Persons with psychiatric disorders 15. other patients who are judged to be exempted by the principal investigator/associate investigator

Design outcomes

Primary

MeasureTime frame
Bispectral index (with a cutoff value of 60)

Secondary

MeasureTime frame
Bispectral index (50 and 70 as cutoff values, respectively)

Contacts

Public ContactKensuke Kobayashi

Hamamatsu University Hospital

kopaken@hama-med.ac.jp+81-53-435-2738

Outcome results

None listed

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