Phase 4Completed
Patient-Controlled Sedation in Port Implantation (PACSPI-2)
Patient-Controlled Sedation in Port Implantation (PACSPI-2) -a Randomized Controlled Trial
- Sponsor
- Region Jönköping County (Government)
- Enrollment
- 340 enrolled
- Conditions
- Pain; Patient Satisfaction; Cancer; Venous Puncture
- Interventions
- Propofol + Alfentanil
- Ages
- adults, older adults
- Registry
- NCT05688384
Full record on ClinicalTrials.gov
From the registry
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 implantation under local anaesthesia Study group: will do SVP implantation under local anaesthesia and patient-controlled sedation. The patients are asked to complete a questionnaire postoperatively which contains questions on pain perception and satisfaction.
Primary outcomes
- Maximal intraprocedural pain level on numeric rating scale
History
Last registry update
Primary completion
Started
Registered