MedTrace Logo

Neurological Events and Unforeseen Risks After Locoregional-anesthesia

NCT07238933 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 3396

Last updated 2025-11-20

No results posted yet for this study

Summary

This is a multicenter, prospective, observational study aimed at determining the incidence of neurological and non-neurological complications following locoregional anesthesia procedures. The study will collect data on events such as nerve injury, hematoma, pneumothorax, and local anesthetic systemic toxicity.

Conditions

  • Regional Anesthesia
  • Regional Anesthesia Block

Interventions

OTHER

Observational assessment after regional anesthesia

Adult patients undergoing single-shot regional anesthesia, including: Upper limb blocks - interscalene, superior trunk, supraclavicular, infraclavicular (coracoid, retroclavicular, costoclavicular), suprascapular (anterior, posterior), axillary, and superficial/intermediate/deep cervical plexus blocks. Lower limb blocks - lumbar, sacral, fascia iliaca (supra/infrainguinal), adductor canal, PENG, femoral, femoral triangle, sciatic (anterior, transgluteal, infragluteal, popliteal), nerve to vastus medialis, genicular, IPACK, common peroneal, ankle, and pudendal blocks. Fascial plane blocks - rectus sheath, ilioinguinal/iliohypogastric, TAP (standard/subcostal/midaxillary), ESP, serratus anterior (deep/superficial), parasternal intercostal (superficial/deep), interpectoral, transversalis fascia, rhomboid intercostal, retrolaminar, quadratus lumborum (anterior/lateral/posterior), paravertebral, intertransverse process, and pectoserratus blocks.

Sponsors & Collaborators

  • Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva

    lead OTHER

Principal Investigators

  • Alessandro De Cassai Prof., MD · UOC Istituto di Anestesia e Rianimazione, Azienda Ospedale Università di Padova

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-12-01
Primary Completion
2027-01-01
Completion
2027-01-01

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07238933 on ClinicalTrials.gov