NCT07238933 Neurological Events and Unforeseen Risks After Locoregional-anesthesia
| NCT ID | NCT07238933 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva |
| Condition | Regional Anesthesia |
| Study Type | OBSERVATIONAL |
| Enrollment | 3,396 participants |
| Start Date | 2026-02-18 |
| Primary Completion | 2027-01-01 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 3,396 participants in total. It began in 2026-02-18 with a primary completion date of 2027-01-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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.
Eligibility 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.
Contact & Investigator
Alessandro De Cassai Prof., MD
PRINCIPAL INVESTIGATOR
UOC Istituto di Anestesia e Rianimazione, Azienda Ospedale Università di Padova
Frequently Asked Questions
Who can join the NCT07238933 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Regional Anesthesia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07238933 currently recruiting?
Yes, NCT07238933 is actively recruiting participants. Contact the research team at ricerca@siaarti.it for enrollment information.
Where is the NCT07238933 trial being conducted?
This trial is being conducted at Bergamo, Italy, Brescia, Italy, Rozzano, Italy, Padova, Italy.
Who is sponsoring the NCT07238933 clinical trial?
NCT07238933 is sponsored by Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva. The principal investigator is Alessandro De Cassai Prof., MD at UOC Istituto di Anestesia e Rianimazione, Azienda Ospedale Università di Padova. The trial plans to enroll 3,396 participants.