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First received: December 16, 2022

Clinical Trial: Patient-Controlled Sedation in Port Implantation (PACSPI-2)

Study Status: COMPLETED

Recruit Status: COMPLETED

Condition: Pain

Study Type: INTERVENTIONAL


Official Title: Patient-Controlled Sedation in Port Implantation (PACSPI-2) -a Randomized Controlled Trial

Brief Summary: The goal of the study is to determine if patient-controlled sedation (PCS) with propofol and alfentanil reduces patient-reported pain perception during implantation of subcutaneous venous port (SVP).The main question it aims to answer: How much pain did you (patient) experience during SVP-implantation Several other questions will be answered regarding: patient´s perception of the procedure, complication rate, procedure data.The study contains two groups which will be compared.Control group: will do SVP…

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