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Comparison of Different Techniques on First Attempt Success in Difficult Vascular Access Patients

NCT04821362 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 270

Last updated 2021-12-03

Study results available
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Summary

The aim of this study is to investigate whether there is any difference between the use of standard techniques, ultrasonography and infra-red light for the success of the first attempt in difficult peripheral vascular access patients. Patients who have difficult vascular access history ( often need 2 or more attempt to access peripheral intravenous catheter), who do not have palpable or visible vein after tourniquet, and who have the hard anticipation according to operator ( easy-moderate-hard) are included to study. The primary objective is planned as the determination of the success rate in the first attempt. Secondary aims of the study were determined as: total procedure time,total number of attempts, and need for rescue procedure

Conditions

  • Vascular Access

Interventions

DEVICE

Ultrasound group

In the ultrasound group, the nurses will insert the cannulas to the peripheral veins as horizontally and longitudinally with the linear probe.

DEVICE

Near Infrared Device Group

In the near infrared device group, the nurses will insert the cannulas to the peripheral veins with AccuVein AV 400.

Sponsors & Collaborators

  • Ege University

    lead OTHER

Principal Investigators

  • Özge Can, MD · Ege University

  • İlhan Uz, MD · Ege University

  • Gülbin Konakçı, Asst. Prof. · Izmir Demokrasi University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-04-15
Primary Completion
2020-02-01
Completion
2020-03-01

Countries

  • Turkey (Türkiye)

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 NCT04821362 on ClinicalTrials.gov