Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Improving pain control after abdominal aortic aneurysm surgery

Official title: Post-Operative Pain Control After Aortic EndoaneurYsmEctomy

Run by IRCCS Policlinico S. Donato · NCT06244732 · Data updated 2026-11-12

This study tests which pain relief method works better for adults after surgery for abdominal aortic aneurysms: an epidural or a series of injections in the abdominal muscles.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorIRCCS Policlinico S. Donato
Academic / other
Locations1 site (San Donato Milanese, Milan)
StatusRecruiting
StartedFebruary 19, 2024
Main results expectedFebruary 2027
Study endsMarch 2027
Registry record updatedJuly 2, 2026
Trial IDNCT06244732 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adult patients over 18 years old who are scheduled for elective open surgical treatment of an abdominal aortic aneurysm.

Probably not a fit

Patients who are pregnant, have chronic pain, or have contraindications to the analgesic methods will 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 evaluates postoperative pain management in adult patients undergoing elective open abdominal aortic aneurysm repair. It compares two methods of analgesia: epidural analgesia and repeated rectus fascia blocks. The goal is to determine which method provides better pain control and reduces complications associated with postoperative pain. The study is conducted in a single center and involves randomizing patients to receive one of the two analgesic techniques.

Why it matters

Potential benefit: If successful, this study could lead to improved pain management and faster recovery for patients undergoing abdominal aortic aneurysm surgery.

How similar studies have gone: Previous studies have shown that multimodal analgesia, including epidural analgesia, can improve postoperative pain management, suggesting this approach has potential for success.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* adult patients (age \> 18 years)
* patients who have given their consent to participate in the study
* patients undergoing elective "open" surgical treatment of an abdominal aortic aneurysm with a midline xipho-pubic incision.

Exclusion Criteria:

* Pregnant women
* Patients being treated for chronic pain
* Known allergy to drugs included in analgesia protocols
* Contraindications to the use of one of the two methods provided:

  * refusal by the patient
  * infection at the puncture site
  * coagulopathy:

    1. PTT \> 40 s and/or INR \> 1.4
    2. platelet count \< 50,000/µL
    3. taking antiplatelet or anticoagulant drugs that have not been discontinued in good time, according to international guidelines
* Emergent intervention
* Lack of consent to participate in the study

Where it's running

  • I.R.C.C.S. Policlinico San Donato
    San Donato Milanese, Milan, Italy
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.