Clinical trial Recruiting at 1 site Observational Ages 18 and up

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 typeObservational
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorUniversity Hospital, Angers
Government
Locations1 site (Angers)
StatusRecruiting
StartedSeptember 14, 2026
Main results expectedFebruary 14, 2027
Study endsMarch 14, 2027
Registry record updatedSeptember 22, 2026
Trial IDNCT07638514 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

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.