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 type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | IRCCS Policlinico S. Donato Academic / other |
| Locations | 1 site (San Donato Milanese, Milan) |
| Status | Recruiting |
| Started | February 19, 2024 |
| Main results expected | February 2027 |
| Study ends | March 2027 |
| Registry record updated | July 2, 2026 |
| Trial ID | NCT06244732 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
- Study coordinator: Mattia Ricotti
- Email: mattia.ricotti@grupposandonato.it
- Phone: +390252774236
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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.