Opioid-free anesthesia for abdominal surgery
Official title: Opioid-free Anesthesia as an Alternative to General Anesthesia in Abdominal Surgery
Run by Jagiellonian University · NCT06380244 · Data updated 2026-11-12
This study is testing whether using an opioid-free anesthesia for abdominal surgery can help patients feel less pain and have fewer side effects compared to traditional anesthesia that includes opioids.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 600 (estimated) |
| Sponsor | Jagiellonian University Academic / other |
| Locations | 1 site (Krakow, Lesser Poland Voivodeship) |
| Status | Recruiting |
| Started | April 29, 2024 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | August 26, 2026 |
| Trial ID | NCT06380244 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients scheduled for abdominal surgery who consent to participate in the study.
✕Probably not a fit
Patients who refuse to participate, cannot operate a PCA pump, or have hypersensitivity to anesthetic drugs may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study aims to compare the effectiveness of opioid-free anesthesia versus traditional general anesthesia in patients undergoing abdominal surgery. Participants will be randomly assigned to receive either an opioid-free protocol using medications like Ketamine, Lignocaine, and Dexmedetomidine, or a combined general anesthesia that includes opioids. The primary focus is on assessing pain levels during the first 48 hours post-surgery, as well as measuring total opioid consumption and evaluating postoperative nausea and vomiting. This approach seeks to determine if avoiding opioids can lead to better long-term outcomes, particularly for cancer patients.
Why it matters
Potential benefit: If successful, this approach could significantly reduce chronic postoperative pain and improve quality of life for surgical patients.
How similar studies have gone: While opioid-free anesthesia is used in practice, there is limited conclusive scientific data confirming its advantages specifically for abdominal surgery, making this study a novel investigation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged 18-75 years scheduled for elective urological surgery under general anesthesia: laparoscopic or robotic nephrectomy, laparoscopic or robotic prostatectomy, or laparoscopic or robotic cystectomy. * Ability to operate a patient-controlled analgesia (PCA) pump postoperatively. * Ability to understand and use the Numeric Rating Scale (NRS) for pain assessment. * Written informed consent. Exclusion Criteria: * Patient's refusal to participate. * Inability to operate the PCA pump. * Inability to understand the NRS pain scale. * Known hypersensitivity to any of the study drugs (anesthetics, ketamine, dexmedetomidine, ropivacaine, oxycodone, metamizole, paracetamol, ibuprofen). * Second- or third-degree atrioventricular block, or symptomatic bradycardia. * Chronic opioid use. * Contraindication to the planned regional anesthesia technique (e.g. coagulopathy or therapeutic anticoagulation, infection at the puncture site).
Where it's running
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Jagiellonian University
Krakow, Lesser Poland Voivodeship, Poland Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.