DIFFICULT INTRAVENOUS ACCESS IN ADULTS (VENSCORE) (VENSCORE)

April 2, 2019 updated by: University Hospital, Bordeaux

DIFFICULT PERIPHERAL INTRAVENOUS ACCESS IN ADULT DURING THE PREOPERATIVE PERIOD

The objective of the prospective multicenter observational study consists in defining a difficult intravenous access score in adult, during the preoperative period.

The main objective: the outcome of interest is defined as failure of cannulation on first attempt.

The risk factors of failure of cannulation on first attempt will be described. Adjusted multivariate models will be constructed. A prediction model will be proposed according to the transparent reporting of a multivariable prediction model for individual prognosis or diagnosis (TRIPOD)

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Objectives:

To define a difficult intravenous access score in adult during the preoperative period Methods Multicenter, Observational prospective study

Patients:

patients >18 years old, undergoing peripheral IV placement just before a surgery in operating room excision criteria: pregnant woman, induction of anesthesia with sevoflurane, Predictor variables include: history of patient (age,BMI, Fitzpatrick skin type, cancer, ICU stay, burn, diabetes, kidney disease, anxiety of patient...) , operator experience characteristics( years since graduation, years of anesthesiology experience, IVs started per month), type of catheter and place of catheterization),and postcatheterization data (success on fist attempt yes or no, number of total attempts until success...)

Study Type

Observational

Enrollment (Actual)

3300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Agen, France
        • Centre Hospitalier d'Agen
      • Ares, France
        • Centre Médico-chirurgical Wallerstein
      • Bayonne, France
        • Centre Hospitalier de la Côte Basque
      • Bordeaux, France, 33000
        • Institut Bergonie
      • Bordeaux, France
        • Centre hospitalier Universitaire de Bordeaux
      • Bordeaux, France
        • Hôpital d'Instruction des Armées Robert Picqué
      • Bordeaux, France, 33000
        • Clinique Saint Augustin Bordeaux
      • Dax, France
        • Centre Hospitalier de Dax
      • La teste de buch, France, 33260
        • Centre Hospitalier d'Arcachon
      • Lagon, France
        • Centre Hospitalier Sud Gironde
      • Libourne, France
        • Centre Hospitalier de Libourne
      • Mont de Marsan, France, 40000
        • Centre Hospitalier de Mont de Marsan
      • Pau, France
        • Centre Hospitalier De Pau
      • Périgueux, France
        • Centre Hospitalier de Perigueux
      • Tahiti, France
        • Centre Hospitalier de Tahiti
    • Ile De La Réunion
      • Saint Pierre La Réunion, Ile De La Réunion, France
        • CHU Saint Pierre

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients undergoing peripheral intravenous placement just before a surgery will be enrolled. (the investigator does not assign specific interventions to the subjects of the study)

Description

Inclusion Criteria:

  • patients >18 years old, undergoing peripheral IV placement just before a surgery in operating room

Exclusion Criteria:

  • patients who refused IV placement; pregnant woman; induction of anesthesia with sevoflurane without venous access in place

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
failure intravenous placement on the first attempt
Time Frame: during the hour before surgery
during the hour before surgery

Secondary Outcome Measures

Outcome Measure
Time Frame
risk factors associated with failure intravenous catheterization
Time Frame: during the hour before surgery
during the hour before surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Bordeaux

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2016

Primary Completion (Actual)

June 1, 2018

Study Completion (Actual)

June 1, 2018

Study Registration Dates

First Submitted

May 24, 2016

First Submitted That Met QC Criteria

May 26, 2016

First Posted (Estimate)

June 2, 2016

Study Record Updates

Last Update Posted (Actual)

April 4, 2019

Last Update Submitted That Met QC Criteria

April 2, 2019

Last Verified

March 1, 2019

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • CHUBXSAR32016-01

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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