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A Workflow and Satisfaction Study Evaluating the Implementation of a New "Smart" Ambulatory Infusion System

NCT01997099 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 62

Last updated 2015-11-05

No results posted yet for this study

Summary

The purpose of this study is to describe the home healthcare organization ambulatory infusion pump programming workflow and the process that was followed to introduce the new CADD®-Solis VIP System to each home healthcare organization or facility. In addition, this study will characterize the overall clinician (Phase 1) and patient (Phase 2) ease of use and satisfaction with the CADD®-Solis VIP System.

Conditions

  • Home Healthcare Organizations Utilizing Ambulatory Infusion Pumps
  • Patients Requiring Infusion With an Ambulatory Infusion Pump

Interventions

DEVICE

CADD®-Solis VIP Pump

DEVICE

CADD™ Solis Medication Safety Software Administrator

Sponsors & Collaborators

  • Smiths Medical, ASD, Inc.

    lead INDUSTRY

Principal Investigators

  • Thomas D Brown, MBA, PharmD · Thomas Jefferson University Hospital - Jefferson Home Infusion

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2015-10-31
Completion
2015-10-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01997099 on ClinicalTrials.gov