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Midline Catheter and Its Impact on Central Lines Removal in ICU

NCT03675711 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 83

Last updated 2023-03-22

No results posted yet for this study

Summary

The study will evaluate 2 strategies to remove central venous catheter (CVC): in one part, the insertion of a midline catheter and in the other part, the conventional insertion of peripheral venous catheter (PVC)

Conditions

  • Vascular Access Device

Interventions

DEVICE

Midline

Patient will receive a Midline catheter within 48h after disappearance of indication for CVC

DEVICE

PVC

Patient will receive a standard PVC within 48h after disappearance of indication for CVC

Sponsors & Collaborators

  • Centre Hospitalier Departemental Vendee

    lead OTHER

Principal Investigators

  • angelina robert · CHD vendee

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-02
Primary Completion
2023-01-03
Completion
2023-01-13

Countries

  • France

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 NCT03675711 on ClinicalTrials.gov