Central Venous Catheter Clinical Trial
Official title:
Prospective Observational Study on the Safety and Efficacy of Cyanoacrylate Skin Glues to Reduce the Risk of Complications After Insertion of Totally Implantable Central Venous Catheters Port-a-Cath
The use of glue as a device in the implantation of central venous catheters has recently been
introduced into European clinical practice, initially with the aim of blocking bleeding at
the point of exit of the PICCs, but at the same time also to close the cutaneous incision
practiced to create the PORT positioning pocket.
It is possible that the surgical incision created for the insertion of the PORT may undergo
complications such as: local bleeding, infections or wounds of the surgical wound.
A solution to this problem could be the application of the cyanoacrylate dermal glue on the
edges of the surgical wound, after intradermal suture. The glue would have the purpose of
sealing the surgical wound so as to immediately seal the skin incision with hemostatic effect
and create a potential barrier against infections.
Patient's informed consent signature for adhesion at the study will be initially requested.
With their acceptance, parameters will be recorded anonymously in the Case Report Form,
identified by a numeric code, until hospital discharge.
The parameters analized will be related to:
- essential patient data (identification number, gender, age, height weight)
- basic diseases
- associated diseases and risk factors
- origin of the patient (department or home)
- reason for positioning
- hemorrhagic complications detected in the first 24 hours
- hemorrhagic complications detected in the first 7 days
- non-bleeding complications detected at 7 days (local and systemic infections, wound
delescence)
The data wil be transferred to an Excel worksheet, in order to conduct a descriptive analysis
related to every variable
;
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