Impact of Catheter Stabilization on Catheter Micro-Motion and Functio

Not Applicable

• Conditions: Phlebitis; Thrombosis; Cardiovascular - Diseases of the vasculature and circulation including the lymphatic system

• Registration Number: ACTRN12623000328673
• Lead Sponsor: Griffith University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-03-28
• Last Update Posted: 3 April 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

•Female or Male sex
•18-65 years of age
•Not pregnant at time of recruitment and within 48 hrs of Day 1 procedures (self-reported)
•Normal haemotology results as per reference range determined by our laboratory.
•Normal coagulation results as per reference range determined by our laboratory.
•Target cephalic veins readily cannulatable (i.e., equal to approximately 2 mm)
•Able and willing to provide verbal and written consent
•Must be an Australian citizen with current Medicare card

Exclusion Criteria

•History of pro coagulative state / condition (e.g., previous deep vein thrombosis)
•Currently on any anti-coagulant or platelet inhibitor medication. Use of NSAIDs and aspirin will be documented however are not exclusionary.
•Haemophilia or any current or history of bleeding disorder or tendency
•Presence or report of current blood borne disease/infection (e.g., hepatitis, HIV, leukemia, lymphoma)
•Difficult vascular access (i.e., vein must be readily palpable and cannulatable – no less than approximately 2 mm diameter
•Allergy or sensitivity to chlorhexidine gluconate, isopropyl alcohol, latex, or skin adhesives
•BMI less than 18.5 kg/m^2 or greater than 35 kg/m^2
•Positive results for the urine drug screen at screening or check-in (including opiates, methadone, cocaine, amphetamines)
•History or presence of alcoholism (self-reported) or drug abuse within the past 2 years
•A current or previous medical, physical, mental / cognitive disorder or anatomical conditions that, in the opinion of the chief or sub-investigator, would place the patient at risk, would make them unable to perform study procedures or has the potential to confound interpretation of the study results. (e.g., musculo-skeletal injury, chronic back pain)
•Employed by Becton Dickinson, Teleflex Medical, ICUMedical or BBraun (conflict of interest)

Study & Design

• Study Type: Interventional
• Study Design: Not specified