Clinical trial Recruiting at 1 site Interventional Ages 18 to 75

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 typeInterventional
Ages18 Years to 75 Years
SexAll
Enrollment600 (estimated)
SponsorJagiellonian University
Academic / other
Locations1 site (Krakow, Lesser Poland Voivodeship)
StatusRecruiting
StartedApril 29, 2024
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedAugust 26, 2026
Trial IDNCT06380244 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

  • Jagiellonian University
    Krakow, Lesser Poland Voivodeship, Poland
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.