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IV Dislodgement Comparative Effectiveness Study

NCT05602285 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 2

Last updated 2025-05-15

No results posted yet for this study

Summary

The goal of this comparative effectiveness study is to compare IV dislodgement frequency in medical-surgical patients with continuous IV fluids infusing.

The main question it aims to answer are:

1\. To determine if the addition of the break-away IV device within IV tubing and customary IV dressing reduces dislodgment when compared to customary IV dressing alone.

Conditions

  • IVF

Interventions

DEVICE

Dislodgement device

Breakaway device that prevents IV dislodgement

Sponsors & Collaborators

  • The Cleveland Clinic

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-01-04
Primary Completion
2024-12-31
Completion
2024-12-31

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 NCT05602285 on ClinicalTrials.gov