Registry for patients undergoing anesthesia and critical care

Is this trial a fit for you?

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

What this trial studies

This observational study aims to collect comprehensive data from approximately 300,000 patients undergoing anesthesia or intensive care procedures at the IRCCS San Raffaele Scientific Institute over a 10-year period. The registry will gather various information, including demographic details, clinical history, therapeutic measures, and patient satisfaction, all anonymized for research purposes. The goal is to enhance the quality of care and inform future clinical studies by analyzing patient outcomes and treatment standards. Data collection will include follow-ups for certain patients after one year to assess long-term effects.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients undergoing Anesthesia or Critical care
* Signed informed consent.

Exclusion Criteria:

Refused informed consent

Where it's running

• Ospedale San Raffaele di Milano
  Milan, Mi, Italy Recruiting

Study contacts

• Study coordinator: Marina Pieri, MD
• Email: pieri.marina@hsr.it
• Phone: +39022643

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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.