Site Selection of Short Peripheral Venous Catheters

NCT ID: NCT03290573

Last Updated: 2019-01-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

1517 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-09-29

Study Completion Date

2019-01-06

Brief Summary

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Up to 90% of catheters fail before therapy is complete. Improved dwell time of intravenous catheters for even small increments of time would further reduce the number of insertions, staff workloads, and costs. In this study, the investigators investigated whether short peripheral venous catheter site of insertion influence the dwell time.

Detailed Description

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Conditions

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Short Peripheral Venous Catheter

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Dorsum of hand group

short peripheral venous catheter place in the dorsum of the hand

Group Type ACTIVE_COMPARATOR

short peripheral venous catheter

Intervention Type DEVICE

short peripheral venous catheter for infusion therapy in adult patients

Forearm group

short peripheral venous catheter place in the forearm

Group Type EXPERIMENTAL

short peripheral venous catheter

Intervention Type DEVICE

short peripheral venous catheter for infusion therapy in adult patients

Interventions

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short peripheral venous catheter

short peripheral venous catheter for infusion therapy in adult patients

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Age \>18 years
* Expected duration of infusion therapy by short peripheral intravenous catheters \>7 days
* Give written informed consent

Exclusion Criteria

* The peripheral venous catheter was inserted in emergency room or in emergency circumstances
* Bloodstream infection
* Had a peripheral venous catheter already in situ at the baseline
* Altered mental state
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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The First Affiliated Hospital of Zhengzhou University

OTHER

Sponsor Role lead

Responsible Party

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Chuanjie Wu

MD, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Chuanjie Wu, MD

Role: STUDY_CHAIR

The First Affiliated Hospital of Zhengzhou University

Locations

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Suzhou municipal hospital

Suzhou, Anhui, China

Site Status

Xuanwu Hospital Captial Medical University

Beijing, Beijing Municipality, China

Site Status

Guizhou Provincial People's Hospital

Guiyang, Guizhou, China

Site Status

The First Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, China

Site Status

The Fifth Affiliated Hospital of Zhengzhou University

Zhengzhou, Henan, China

Site Status

Xiangtan Central Hospital

Xiangtan, Hunan, China

Site Status

Countries

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China

Other Identifiers

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FAHZU-2017-016

Identifier Type: -

Identifier Source: org_study_id

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