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Comparing Sensitivity and Specificity of Pacemaker ID Application and Cardiac Rhythm Management Device-Finder Application.

A

Aga Khan University Hospital, Pakistan

Status

Completed

Conditions

Cardiac Arrhythmia

Treatments

Other: Device identification using Xray.

Study type

Observational

Funder types

Other

Identifiers

NCT04957108
2020-5101-14156

Details and patient eligibility

About

Smart phone-based applications to identify cardiac implantable electronic devices (CIED) are extremely useful in circumstances where urgent device interrogation is needed and device identification card is not available. Few studies have provided insight regarding the utility of these applications. We have studied two widely available applications i.e., Pacemaker ID app (PMIDa) or Cardiac Rhythm Management Devices-Finder (CRMD-f) to identiy device manufacturers in CIEDs.

Full description

Smart phone-based applications to identify cardiac implantable electronic devices (CIED) are extremely useful in circumstances where urgent device interrogation is needed and device identification card is not available. Few studies have provided insight regarding the utility of these applications. We have studied two widely available applications i.e., Pacemaker ID app (PMIDa) or Cardiac Rhythm Management Devices-Finder (CRMD-f) to identiy device manufacturers in CIEDs.

547 patients who underwent CIED implantation from year 2016 - 2020 in our institute were enrolled. There were 438 Medtronic and 109 St. Jude's devices. All chest radiographs were de-identified and resized into 225*225 pixels focusing on the CIED. PMIDa and CRMD-f applications were used to identify CIED. Accuracy, sensitivity, specificity, negative predictive value, and positive predictive value for both applications were calculated and compared.

Enrollment

547 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients undergoing CIED implantation and having xray post-implant at any point and time.

Exclusion criteria

  • Patients with CIED for whome Xray was not available.

Trial design

547 participants in 1 patient group

All cardiac implantable devices
Description:
Assessed separately by Pacemaker ID app and cardia-x algorithm
Treatment:
Other: Device identification using Xray.

Trial contacts and locations

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Data sourced from clinicaltrials.gov

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