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A comparison of rocuronium potentiation responses to remimazolam, sevoflurane and propofol in eldery : A prospective comparative study.

A comparison of rocuronium potentiation responses to remimazolam, sevoflurane and propofol in eldery : A prospective comparative study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1031240017
Enrollment
48
Registered
2024-04-08
Start date
2024-04-08
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 undergoing general anesthesia

Interventions

The sedative of choice is remimazolam, sevoflurane, or propofol, depending on the envelope method. Blood samples are drawn during general anesthesia.

Sponsors

Takagi Shunichi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients over 65 years 2) Patients with American Society of Anesthesiologists physical status classification 1-3. 3) Patients who receive written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of allergy to muscle relaxants or antagonists 2. Patients with severe complications 3. patients with neuromuscular disease 4. Patients taking medications that may affect the effect of muscle relaxation. 5. Patients who are deemed inappropriate as research subjects by the principal investigator 6. Patients who refuse to participate in the study.

Design outcomes

Primary

MeasureTime frame
PTC appearance time in remimazolam, sevoflurane, and propofol groups

Secondary

MeasureTime frame
T1 and T2 appearance time in sevoflurane, propofol, and remimazolam groups, and time to 100% TOF ratio after sugammadex administration. PTC, and rocuronium-rocuronium protein binding rate in blood at T1 and T2 appearance

Contacts

Public ContactHanae Sato

Nihon University Itabashi Hospital

nakamura.hanae@nihon-u.ac.jp+81-3-3972-8111

Outcome results

None listed

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