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A Single-institutional Study to Assess the Time Efficiency and Working Satisfaction Using ANDY(Automatic Needle Destroyer)

NCT04039906 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 129

Last updated 2019-12-03

No results posted yet for this study

Summary

Evaluate the efficiency of adopting the automated needle processing system by evaluating efficiency, usability and safety when using ANDY(Automatic Needle Destroyer). Install ANDY(Automatic Needle Destroyer) in the ER, and evaluate the system by comparing the efficiency of the work, usability, actual decrease ratio of needlestick injury between using the automated needle processing system and not using it.

Conditions

  • Needle Stick Injuries

Interventions

DEVICE

Removal of needle with using ANDYs

1. ANDY will be provided to medical staffs to be use in removal needles from syringes during 7 days 2. Record the time required for the needle removal procedure by photographing the needle removal procedure during 24 hours/7 days. Identify the number of syringes processed by ANDY. 3. After 3rd week, do survey and interview 15 people selected by the convenient sample method. By interviewing, collect information of overall experience after using automated needle processing system, how long their hospital working experience is, and other information or systems the interviewees felt those are necessary.

Sponsors & Collaborators

  • Samsung Medical Center

    lead OTHER

Principal Investigators

  • TAERIM KIM, Doctoral · Samsung Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-02
Primary Completion
2019-09-23
Completion
2019-09-23

Countries

  • South Korea

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 NCT04039906 on ClinicalTrials.gov