Perineural Catheter for Hindfoot Surgery Pain Control
Official title: A Comparative Evaluation of Postoperative Analgesia Using a Perineural Catheter Versus a Single Nerve Block in Rearfoot Surgery
Run by University Hospital, Angers · NCT07638514 · Data updated 2026-11-12
This study tests whether a continuous perineural catheter delivering local anesthetic after hindfoot surgery helps with pain more than standard care.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | University Hospital, Angers Government |
| Locations | 1 site (Angers) |
| Status | Recruiting |
| Started | September 14, 2026 |
| Main results expected | February 14, 2027 |
| Study ends | March 14, 2027 |
| Registry record updated | September 22, 2026 |
| Trial ID | NCT07638514 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults undergoing hindfoot surgery with the ability to complete questionnaires and ASA I–III are eligible.
✕Probably not a fit
Patients who cannot receive regional anesthesia or who do not tolerate perineural catheter analgesia may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational practice-evaluation audit at the University Hospital of Angers. It uses data from routine care to see how a perineural catheter for continuous local anesthetic infusion affects postoperative pain and recovery after hindfoot surgery. No changes to intraoperative care are made; researchers collect information from standard postoperative practice and patient-reported questionnaires. The goal is to determine if prolonged regional analgesia improves pain outcomes and functional recovery in this setting.
Why it matters
Potential benefit: If successful, patients could experience better pain control and potentially faster recovery after hindfoot surgery.
How similar studies have gone: Regional anesthesia techniques have shown benefit in various orthopedic surgeries, but specific data for hindfoot procedures are limited and further evidence is needed.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patients; * Patients with an American Society of Anesthesiologists physical status (ASA score) of 1, 2, or 3; * Patients who have undergone hindfoot surgery; * Patients capable of completing the questionnaires. Exclusion Criteria: * Contraindications to regional anesthesia (known hypersensitivity to the local anesthetic, infection at the injection site, uncontrolled neurological condition); * Emergency surgery * Cognitive impairment; * Uncontrolled psychiatric condition; * Pregnancy or breastfeeding; * Substance abuse; * Use of neuroleptics or lithium; * Individuals subject to legal guardianship * Individuals deprived of liberty by judicial or administrative order * Patients who object to the study.
Where it's running
-
University Hospital of Angers
Angers, France Recruiting
Study contacts
- Principal investigator: Benjamin DUMARTINET — University Hospital of Angers
- Study coordinator: Benjamin DUMARTINET
- Email: benjamin.dumartinet@chu-angers.fr
- Phone: 241353637
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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.