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/Actively Recruiting
Led by Università Vita-Salute San Raffaele · Updated on 2025-08-06
30000
Participants Needed
1
Research Sites
13 weeks
Total Duration
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
Anesthesia and Critical Care Registry
M
Marina Pieri, MD
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Università Vita-Salute San Raffaele
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - Variable, prior to hospital admission
Participants are screened for eligibility to participate in the trial.
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
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
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Have more questions? Get in touch with our team for quick support
Arthur James, Audrey De Jong, Thomas Jeanmougin...
https://pubmed.ncbi.nlm.nih.gov/35164679/Abi Beane, Jorge I F Salluh, Rashan Haniffa
https://pubmed.ncbi.nlm.nih.gov/34393177/Adrian Liau, Jeana E Havidich, Tracy Onega...
https://pubmed.ncbi.nlm.nih.gov/26579661/William L Lanier
https://pubmed.ncbi.nlm.nih.gov/17120937/Fiona E Kelly, Kevin Fong, Nicholas Hirsch...
https://pubmed.ncbi.nlm.nih.gov/25099838/Yaseen M Arabi, Elie Azoulay, Hasan M Al-Dorzi...
https://pubmed.ncbi.nlm.nih.gov/33616696/Alessandro Belletti, Diego Palumbo, Alberto Zangrillo...
https://pubmed.ncbi.nlm.nih.gov/33678544/Fred E Shapiro, Samir R Jani, Xiaoxia Liu...
https://pubmed.ncbi.nlm.nih.gov/24882129/Philippe Desmarais, Nathan Herrmann, Fahad Alam...
https://pubmed.ncbi.nlm.nih.gov/31337487/Fabrizio Monaco, Alessandro Belletti, Tiziana Bove...
https://pubmed.ncbi.nlm.nih.gov/29709436/Università Vita-Salute San Raffaele
Lead Sponsor