Actively Recruiting
Development of an Arterial Pressure Monitoring Set Fixation Apparatus
Led by Yuzuncu Yil University · Updated on 2025-06-25
60
Participants Needed
1
Research Sites
39 weeks
Total Duration
On this page
Sponsors
Y
Yuzuncu Yil University
Lead Sponsor
A
Ataturk University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to develop an arterial pressure monitoring set fixation device and evaluate its effectiveness in clinical settings. The device is designed to increase the stability and comfort of arterial pressure monitoring during patient care. An experimental study will be conducted with patients requiring arterial pressure monitoring. The device's effectiveness will be evaluated by measuring fixation stability and postoperative arterial blood pressure-CVP parameters over 48 hours. The study aims to demonstrate that the new fixation device can improve patient safety and monitoring accuracy compared to the standard method using adhesive tape, thereby contributing to better clinical outcomes.
CONDITIONS
Official Title
Development of an Arterial Pressure Monitoring Set Fixation Apparatus
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adult patients aged 18-80 years
- Patients undergoing arterial catheterization for invasive blood pressure and CVP monitoring
- Patients able to provide informed consent
- Hemodynamically stable patients undergoing Coronary Artery Bypass Grafting (CABG)
You will not qualify if you...
- Patients younger than 18 or older than 80 years
- Patients with coagulopathy or bleeding disorders
- Patients with local infection or skin lesions at the catheter insertion site
- Patients unable to provide informed consent
- Hemodynamically unstable patients
- Patients with known allergy to device materials or adhesive tapes
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Van Training and Research Hospital
Van, Turkey (Türkiye), 65000
Actively Recruiting
Research Team
Z
ZEYNEP GÜRKAN, Res. Asst.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SEQUENTIAL
Primary Purpose
OTHER
Number of Arms
1
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