Bedside Body Composition for Better Anesthesia Dosing

Point-of-Care Body Composition Analysis for Optimizing Intravenous Anesthetic Dosing

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-jRCT1021250016

Enrollment

Registered

2025-08-25

Start date

2026-07-13

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

There is no specific target disease.

Interventions

none

Eligibility

Inclusion criteria

Inclusion criteria: A total of 33 adult patients scheduled for surgery under general anesthesia with propofol will be included, provided they meet all of the following criteria: 1. ASA (American Society of Anesthesiologists) physical status classification 1-3 2. Patients who provided informed consent to participate in this study 3. Male patients aged 65 years or older 4. Surgical procedures with an expected duration of less than 6 hours

Exclusion criteria

Exclusion criteria: 1. Presence of liver disease 2. Patients with severe arrhythmias 3. Allergy to propofol

Design outcomes

Primary

Measure	Time frame
Performance Error	—

Secondary

Measure	Time frame
MDPE, MDAPE, Wobble, Divergence	—

Contacts

Public ContactShinju Obara

Fukushima Medical University Hospital

masui@fmu.ac.jp+81-245471342

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026