About this trial
The goal of this clinical trial is to determine whether continuous nefopam administration, as part of a multimodal analgesia strategy, reduces opioid consumption and improves patient satisfaction after pancreatoduodenectomy.
The main questions are:
Does nefopam administration reduce opioid consumption after pancreatoduodenectomy?
Does nefopam administration reduce postoperative pain levels after pancreatoduodenectomy?
Researchers will compare two other analgesic strategies, namely continuous lidocaine infusion and epidural analgesia, to assess whether they lead to better outcomes.
Participants will complete the QoR-15 questionnaire and report their pain levels at predefined time points before and after surgery.
Eligibility criteria
Qualifiers
Patients scheduled for elective pancreatoduodenectomy surgery
Agreed to participate in the study
Disqualifiers
Refusal to participate
Emergency surgery
Patients with neurological disorders or other muscular or psychiatric disorders that impede communication
Known allergic reactions to the used medication
Trial design
Treatments tested in this trial
- Nefopam 120mg/day infusion
- Lidocaine Infusion
- Peridural
- Multimodal IV analgesia