Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
3300 participants
OBSERVATIONAL
2016-06-30
2018-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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)
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Accuvein Versus Standard Care for Intravenous Cannulation Procedure in Children
NCT03427723
Evaluation of Accuvein in Adult Patients
NCT01020461
Evaluation of the Occurrence of Acute Complications Caused by a Central Venous Catheter Placement
NCT01405534
Complications Related to Vascular Access Devices in Home Parenteral Nutrition Patients
NCT05948514
Evaluation of Accuvein in Obese Patients
NCT02015845
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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...)
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
peripheral intravenous catheterization
success or failure intravenous placement on first attempt and factors associated with failed intravenous catheterization
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Bordeaux
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Centre Hospitalier Sud Gironde
Lagon, France, France
CHU Saint Pierre
Saint Pierre La Réunion, Ile de La Réunion, France
Centre Hospitalier d'Agen
Agen, , France
Centre Médico-chirurgical Wallerstein
Arès, , France
Centre Hospitalier de la Cote Basque
Bayonne, , France
Clinique Saint Augustin Bordeaux
Bordeaux, , France
Institut Bergonié
Bordeaux, , France
Centre hospitalier Universitaire de Bordeaux
Bordeaux, , France
Hôpital d'instruction des Armées Robert Picqué
Bordeaux, , France
Centre Hospitalier de Dax
Dax, , France
Centre Hospitalier d'Arcachon
La Teste-de-Buch, , 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
Centre Hospitalier de Tahiti
Tahiti, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CHUBXSAR32016-01
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.