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NCT06375252 Clinical Trial

Evaluation of Central Jugular Vein Catheter Lumen Holder Design and Ergonomic Use

Central Venous Catheterization Clinical Trial

— CJVClumen  

Official title:
Evaluation of Central Jugular Vein Catheter Lumen Holder Design and Ergonomic Use

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06375252
Other study ID # sbughfyaseminozkan1985
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date April 19, 2024
Est. completion date May 30, 2024

Study information
Verified date April 2024
Source Saglik Bilimleri Universitesi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to evaluate the design and ergonomic use of central jugular vein catheter lumen holder.

Description:

Central venous catheterisation is one of the invasive procedures commonly used in the treatment and care of patients in internal and surgical clinics and generally in intensive care units and in the follow-up of patients to be operated. Central venous catheters (CVC) are indispensable diagnostic and therapeutic applications in modern medicine. It is a practical method used in cases where venous vessels cannot be used. Central venous catheterisation is a cannula inserted into the subclavian, jugular or femoral vein. Nurses are responsible for the care and daily control of central venous catheters inserted by physicians. Central venous catheterisation is widely used by nurses in clinical wards, intensive care units and during surgical procedures for many indications such as monitoring, drug administration and parenteral nutrition. Subclavian vein and jugular vein are most commonly used for this purpose. Many complications such as haemothorax, pneumothorax, malposition, air embolism and infection may develop during CVC applications. The role of the nurse is very important in the determination of CVC complications. In terms of the individual with a central vein catheter, it constitutes a situation where the individual is worried about a catheter placed in his/her body and needs to be sensitive to the area where it is placed. They should be careful while performing daily life activities with the catheter. The presence of the central jugular vein catheter in the neck area affects the head position, and the sagging of the catheter lumens on the dressing causes skin sensitivity. Individuals with central jugular vein catheters experience some problems such as discomfort due to sagging of the catheter lumens, inability to move comfortably in head and neck movements and sagging of the catheter lumens. The aim of this study was to develop an innovative design of central jugular vein catheter lumen holder to ensure the position, fixation and comfort efficiency of the central jugular vein catheter and to evaluate its ergonomic use.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 40
Est. completion date May 30, 2024
Est. primary completion date May 16, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Being a healthy individual over the age of 18 - Not having had a central jugular vein catheter inserted before for any reason (no experience) - Being literate - Voluntarily agreeing to participate in the research - Being able to carry out daily life activities individually Exclusion Criteria: - Leaving work voluntarily - Limitation in the head and neck area

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Central Jugular Vein Catheter Lumen Holder Apparatus
Participants will experience the central jugular vein catheter lumen holder apparatus, perform walking, sitting, supine, right and left side lying activities and fill out the evaluation forms prepared by the researcher. They will then experience the same activities without the apparatus.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Saglik Bilimleri Universitesi

Outcome
Type Measure Description Time frame Safety issue
Primary demographic information Contains participant identifying information 10 minutes
Secondary comfort effect The participant's comfort level is evaluated with Visual Analog Scale. 30 minutes
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