On-site verification and patient impact investigation of cross check system using ultra high frequency RFID tag and RFID reader

On-site verification and patient impact investigation of cross check system using ultra high frequency RFID tag and RFID reader - On-site verification and patient impact investigation of cross check system using ultra high frequency RFID tag and RFID reader

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000023998

Enrollment

250

Registered

2016-10-01

Start date

2017-01-01

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 with implantable cardiac device

Interventions

From January 2017 to December 2018, admission patients with implantable cardioverter device required the check the unanticipated setting change before and after admission and check the unanticipated s

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: All patients within the age limit

Exclusion criteria

Exclusion criteria: Only age

Design outcomes

Primary

Measure	Time frame
existence or non-existence of unanticipated setting change of implantable cardiac device	—

Secondary

Measure	Time frame
existence or non-existence of nursing work alleviation	—

Countries

Japan

Contacts

Public ContactClinical research ethical review committee Mie university hospital

Mie university hospital Clinical research ethical review committee

s-kenkyu@clin.medic.mie-u.ac.jp059-232-1111

Outcome results

None listed

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