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Accuracy study of bladder ultrasound equipment.

Accuracy study of A-mode bladder ultrasound devices in healthy volunteers

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-jRCTs062210073
Enrollment
6
Registered
2022-01-31
Start date
2022-02-27
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

none

Interventions

1.After injecting saline solution, measure the intravesical urine volume using "General-purpose echo (TOSHIBA Xario200, device name: TUS-X200)", "Lilliam One", "Lilliam IP200", and "Lilliam Spot 2" ea

Sponsors

Sato Yuzuri
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1)Healthy male, aged from 20 to 39 (2)Those who are judged to be healthy with less than 100 mL of residual urine in the bladder based on the echo (general-purpose echo) measurement value of the ultrasonic diagnostic imaging device for the bladder performed after obtaining consent.

Exclusion criteria

Exclusion criteria: (1)Subject with lower urinary tract disorder (2)Subject judged by a doctor to have a lot of residual urine by general-purpose echo (3)Subject determined to be ineligible by the principal investigator

Design outcomes

Primary

MeasureTime frame
Measurements of each of the four modality including general purpose echo for intravesical saline (1) Comparison between the measured value of intravesical urine volume by ultrasound and the volume of urinary catheterization (2) Time required for measurement (3) Reproducibility of each measuring device (4) Posture effect(Only Lilium-SPOT 2) (5) Impact of measurer(Only Lilium-SPOT 2)

Contacts

Public ContactRyoji Sugiura

MAX INTEGRA JAPAN Co., Ltd.

sugiura@airinter.jp+81-90-3433-0055

Outcome results

None listed

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