Clinical trial Recruiting at 1 site Observational Ages 18 and up

Neurological and systemic risks after locoregional anesthesia

Official title: Neurological Events and Unforeseen Risks After Locoregional-anesthesia

Run by Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva · NCT07238933 · Data updated 2026-11-12

This study tests how often nerve injuries, pneumothorax, and other complications occur after a single-shot regional nerve or fascial plane block in adults.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment3396 (estimated)
SponsorSocieta Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva
Academic / other
Locations4 sites (Bergamo, Bergamo and 3 other locations)
StatusRecruiting
StartedFebruary 18, 2026
Main results expectedJanuary 1, 2027
Study endsJanuary 1, 2027
Registry record updatedSeptember 11, 2026
Trial IDNCT07238933 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 or older scheduled for a single-shot nerve or fascial plane block.

Probably not a fit

Patients receiving multiple blocks or catheter-based techniques are not expected to benefit from study findings.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This multicenter, prospective observational study collects data on complications following locoregional anesthesia, including nerve injury, hematoma, pneumothorax, and local anesthetic systemic toxicity. It focuses on single-shot blocks in upper and lower limbs and fascial plane blocks to estimate incidence and explore potential risk factors. Data are gathered from routine clinical care across several Italian centers, with standardized follow-up to identify both neurological and non-neurological events. The goal is to better understand the true safety profile of locoregional anesthesia and identify factors that may predict adverse outcomes.

Why it matters

Potential benefit: If successful, the study could provide clearer information on the risks of locoregional anesthesia to improve patient counseling and safety.

How similar studies have gone: Previous small studies and registries have suggested rare complications; this study aims to provide more robust, prospective incidence data.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age ≥ 18 years.
* Scheduled to undergo a single-shot nerve or fascial plane block.
* Ability to provide written informed consent.

Exclusion Criteria:

* Performance of more than one single-shot nerve or fascial plane block within the same anatomical region or sensory distribution during the same procedure.
* Use of continuous nerve or fascial plane catheter-based anesthesia.
* Presence of a language barrier that, in the investigator's judgment, would prevent adequate follow-up.

Where it's running

  • Azienda Ospedale-Università Padova
    Padova, Padova, Italy
    Recruiting
  • ASST Papa Giovanni XXIII
    Bergamo, Bergamo, Italy
    Not yet recruiting
  • Spedali Civili di Brescia
    Brescia, Brescia, Italy
    Not yet recruiting
  • Irccs Humanitas Research Hospital
    Rozzano, Milan, Italy
    Not yet recruiting

Study contacts

  • Principal investigator: Alessandro De Cassai Prof., MD — UOC Istituto di Anestesia e Rianimazione, Azienda Ospedale Università di Padova
  • Study coordinator: Cristina Cacciagrano Clinical Reasearch Office SIAARTI
  • Email: ricerca@siaarti.it
  • Phone: +39 06 4452816

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.