Intravenous Cannulation Using Vein Display Instrument and Without Using Vein Display Instrument in Pediatric Patients

Comparison Between Using Vein Display Instrument and Without Using Vein Display Instrument for Successful Intravenous Cannulation in Pediatric Patients

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03134560

Enrollment

Registered

2017-05-01

Start date

2016-04-30

Completion date

2016-05-31

Last updated

2017-10-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Difficult Vein Access

Keywords

vein display instrument, pediatric, vein access, vein cannulation

Brief summary

This study aims to compare intravenous cannulation success rate between using vein display instrument and without using vein display instrument in pediatric patients.

Detailed description

Approval from Ethical Committee of Faculty of Medicine Universitas Indonesia was acquired prior conducting the study. Parents' subjects were given informed consent before enrolling the study. After doing asepsis and antisepsis procedure and putting on the tourniquet the first group would get intravenous cannulation without vein displaying instrument. While for the second group, after doing asepsis procedure and tourniquet was put on, a vein display instrument was used to choose the vein. Intravenous cannulation was done after antiseptic procedure. After blood dripped out of the cannula, cannula was connected to the infusion set. Evaluation was done to assess vein route establishment, canulation attempt number and swelling. Data recorded were analyzed using Statistical Package for the Social Sciences (SPSS) using Chi-square test or Fisher Exact test. Significant value is p\<0.05.

Interventions

DEVICEVein Display Instrument

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

SUPPORTIVE_CARE

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

No minimum to 5 Years

Healthy volunteers

Inclusion criteria

* Subjects aged 0-5 years old * Subjects with difficult vein access (e.g. edema, obesity, chemotherapy history), * Subjects whose parents had signed the informed consent * Subjects with available vein access locations at the back of either hands.

Exclusion criteria

* Subjects who had infection signs at the designated vein access location * Subjects in need of emergency procedures. Drop out Criteria: * Subjects resigned from the study * Subjects rejected any next attempt of intravenous cannulation * Subjects who received anesthetic drugs before intravenous cannulation.

Design outcomes

Primary

Measure	Time frame	Description
Successful first vein cannulation attempt	Day 1	Whether the first vein cannulation attempt successful or not will be recorded

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026