A pilot study that evaluates the efficacy of the wireless device to detect a patient's self-extraction of an intravascular tube and informs a nurse or doctor in charge.

A pilot study that evaluates the efficacy of the wireless device to detect a patient's self-extraction of an intravascular catheter or a nasogastric tube and informs a nurse or doctor in charge. - A study that evaluates the efficacy of the device to detect a patient's self-extraction of an IV tube or a NG tube and informs a nurse or doctor.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000050243

Enrollment

Registered

2023-02-07

Start date

2023-02-07

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

higher brain dysfunction

Interventions

To use a test device

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who are 70 years or older, have altered mental status, dementia, a history of psychiatric diseases, a history of delirium, an extraction of an IV tube or nasogastric tube, or a possibility of extracting a tube.

Exclusion criteria

Exclusion criteria: In case a patient or his/her legal guardian does not consent to participating in this study

Design outcomes

Primary

Measure	Time frame
Success in detection and prevention, failure of detection, incorrect detection, success in detection but failure in prevention	—

Countries

Japan

Contacts

Public ContactShinya Miyamoto

International University of Health and Welfare Atami Hospital Department of Neurosurgery

shinyamiyamoto@hotmail.com0557819171

Outcome results

None listed

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

A pilot study that evaluates the efficacy of the wireless device to detect a patient&#39;s self-extraction of an intravascular tube and informs a nurse or doctor in charge.