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Clinical Trials in the USA / NCT06623318
Recruiting Not applicable

IV Ensure in Patients Receiving OPAT

NCT06623318 · tracked via the Priya Life Science USA tracker
Sponsor
IV Ensure
Phase
Not applicable
Started
2023-08-23
Last updated
2024-10-02

Condition(s) studied

Determine If Adherence Rates with IV Antibiotics in OPAT Have a Correlation to Hospital Readmission Rates

Investigational drug(s) / intervention(s)

Remote therapeutic monitoring device

Remote therapeutic monitoring device: IV Ensure proprietary remote therapeutic monitoring device is used to record and transmit data associated with date, time, and duration of IV medications administered in the home setting post-acute.

Study summary

The purpose of remote therapeutic monitoring is to provide oversight and evaluation of patients receiving IV medications in the home setting post-acute. The goal is to improve patient outcomes and decrease re-admission rates for related diagnoses due to poor adherence. Remote therapeutic monitoring provides data used in the determination of dates, times, and duration of doses administered in the home setting to support real-time intervention by dedicated care managers to support improved adherence with prescribed dosing regiments. The objectives of the study are to:

1. Determine adherence rates for IV medications administered in the home.
2. Assess re-admission against adherence rates.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Adult patients enrolled in OPAT (IV antibiotic therapy) discharged to the home setting will be included in the study. Exclusion Criteria: * Patients enrolled in OPAT (IV antibiotic therapy) discharged to nursing homes, SNF (Skilled Nursing Facility), and pediatric patients will be excluded from the study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The University of Oklahoma Health Sciences Center Oklahoma City Oklahoma Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06623318 on ClinicalTrials.gov ↗ ← All trials in the USA