Comparison of Application Effects Between Long- and Standard Short- Peripheral Venous Catheters

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorShenzhen Third People's Hospital

About this trial

Short PIVC (intravenous indentation needle) accounts for more than 50% of clinical infusion tools, but long PIVC is rarely used and studied in China. This study aims to explore the application characteristics and application effects of long PIVC in China. It provides reference for the correct selection of infusion tools, and promotes the clinical application and promotion of new intravenous therapy tools.

The study nurse will work with the responsible physician to assess the eligibility for enrollment and sign the informed consent. Were randomly assigned to the control group (to receive a new 24G/22G (0.7mm\*19mm/0.9mm\*25mm) short PIVC (closed needle protected venous catheter system) puncture) or the intervention group (to insert a new 3F (8cm) or 4F(10cm) long PIVC) for daily routine maintenance until catheter removal, General demographic data, laboratory-related data, catheter-related data, catheter-related complications (unplanned extubation, phlebitis, catheter blockage, catheter-related thrombosis, catheter-related bloodstream infection, exudation, etc.) and patient satisfaction were collected.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

A male or female aged 18 years or older who is able and willing to give written informed consent;

Identification of the patient's medical diagnosis based on the competent physician and the study nurse at any time during the hospital stay, and judgment that the duration of peripheral intravenous infusion therapy needs to exceed 4 days;

Subjects with good compliance and can cooperate with catheter maintenance and observation.

Disqualifiers

Patients who are delirious and unable to cooperate;

Patients requiring central venous access;

Patients suffering from connective tissue diseases or blood diseases;

Patients allergic to catheters or dressings;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Long peripheral venous catheter

    Device

    In this study, patients eligible for admission were subjected to peripheral vein long catheter puncture according to the operating standards, daily routine maintenance until catheter removal, and relevant data were collected.

  • Control group (Short peripheral venous catheter)

    Other intervention

    In this study, the patients eligible for admission will undergo peripheral venous short catheter puncture according to the operating standards, daily routine maintenance until catheter removal, and relevant data will be collected.

Treatment groups

250 Participants
are divided into 2 treatment groups
Group A: Intervention groupExperimental treatment 1 intervention
Group B: Control groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Unplanned extubation

Any complications of catheter removal before completion of IV therapy or before the recommended time of catheter use. Removal of the catheter at the end of intravenous infusion therapy is not considered catheter failure.

Time frame
Up to 2 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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