DIFFICULT INTRAVENOUS ACCESS IN ADULTS (VENSCORE)

Peripheral Venous Catheterization Clinical Trial

— VENSCORE  

Official title:

DIFFICULT PERIPHERAL INTRAVENOUS ACCESS IN ADULT DURING THE PREOPERATIVE PERIOD

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02789046
• Other study ID #: CHUBXSAR32016-01
• Status: Completed
• Start date: June 2016
• Est. completion date: June 2018

Study information

• Verified date: March 2019
• Source: University Hospital, Bordeaux
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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)

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...)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3300
• Est. completion date: June 2018
• Est. primary completion date: June 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Peripheral Venous Catheterization

Intervention

Procedure:
• peripheral intravenous catheterization
success or failure intravenous placement on first attempt and factors associated with failed intravenous catheterization

Locations

Country	Name	City	State
France	Centre Hospitalier d'Agen	Agen
France	Centre Médico-chirurgical Wallerstein	Ares
France	Centre Hospitalier de la Cote Basque	Bayonne
France	Centre hospitalier Universitaire de Bordeaux	Bordeaux
France	Clinique Saint Augustin Bordeaux	Bordeaux
France	Hôpital d'instruction des Armées Robert Picqué	Bordeaux
France	Institut Bergonié	Bordeaux
France	Centre Hospitalier de Dax	Dax
France	Centre Hospitalier d'Arcachon	La teste de buch
France	Centre Hospitalier Sud Gironde	Lagon
France	Centre Hospitalier de Libourne	Libourne
France	Centre Hospitalier de Mont de Marsan	Mont de Marsan
France	Centre Hospitalier de Pau	Pau
France	Centre Hospitalier de Périgueux	Périgueux
France	CHU Saint Pierre	Saint Pierre La Réunion	Ile De La Réunion
France	Centre Hospitalier de Tahiti	Tahiti

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	failure intravenous placement on the first attempt		during the hour before surgery
Secondary	risk factors associated with failure intravenous catheterization		during the hour before surgery