Actively Recruiting

Age: 18Years +
All Genders
ID06033404

Registry of Patients Undergoing Anesthesia or Intensive Care Maneuvers

Led by Università Vita-Salute San Raffaele · Updated on 2025-08-06

30000

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are collecting data from about 300,000 patients who undergo anesthesia or intensive care procedures at a scientific institute over a 10-year period. The goal is to create a detailed registry to support studies aimed at improving treatments and patient care in these fields. This observational study follows ethical guidelines and requires informed consent from participants. The study collects a wide range of information, including patient demographics, medical history, details about anesthesia and intensive care treatments, laboratory results, diagnostic tests, therapeutic procedures, patient satisfaction, and evaluation scales. All data will be anonymized before being added to the registry to protect patient privacy. Participants are observed during their hospital stay, from admission until discharge, which usually happens within 30 days. For some patients, follow-up by phone may occur after one year. Researchers analyze the data to understand patient outcomes related to anesthesia and critical care. Participation is voluntary, and no extra costs are expected for patients.

CONDITIONS

Brief Title

Anesthesia and Critical Care Registry

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing Anesthesia or Critical care
  • Signed informed consent.
Not Eligible

You will not qualify if you...

  • Refused informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - Variable, prior to hospital admission

Participants are screened for eligibility to participate in the trial.

Monitoring

Duration - From hospital admission until discharge (usually up to 30 days)

Participants who undergo routine anesthesia or critical care procedures are observed during their hospital stay. Data related to clinical history, therapeutic measures, laboratory parameters, diagnostic tests, and patient evaluations are collected.

Data collected throughout hospital stay

Long-term Monitoring

Duration - Up to 1 year after discharge

For certain categories of participants, follow-up is conducted by telephone to assess clinical outcomes one year after hospital discharge.

1 telephone follow-up visit

Trial Site Locations

Total: 1 location

1

Ospedale San Raffaele di Milano

Milan, MI, Italy, 20132

Actively Recruiting

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Research Team

M

Marina Pieri, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Frequently Asked Questions

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Published Research Related To This Trial

Characteristics and outcomes of patients undergoing anesthesia while SARS-CoV-2 infected or suspected: a multicenter register of consecutive patients.

Arthur James, Audrey De Jong, Thomas Jeanmougin...

https://pubmed.ncbi.nlm.nih.gov/35164679

Extracorporeal Membrane Oxygenation: Beyond Cardiac Surgery and Intensive Care Unit: Unconventional Uses and Future Perspectives.

Fabrizio Monaco, Alessandro Belletti, Tiziana Bove...

https://pubmed.ncbi.nlm.nih.gov/29709436