Registry for patients undergoing anesthesia and critical care
Registry of Patients Undergoing Anesthesia or Intensive Care Maneuvers
This study is collecting information from around 300,000 patients who are having anesthesia or critical care to see how their treatment affects their health and satisfaction over time.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 30000 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Università Vita-Salute San Raffaele Academic / other |
| Locations | 1 site (Milan, MI) |
| Trial ID | NCT06033404 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are patients who are scheduled to undergo anesthesia or critical care procedures and can provide informed consent.
Not a fit: Patients who refuse to provide informed consent will not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could significantly improve patient management and therapeutic standards in anesthesia and critical care.
How similar studies have performed: Other registry studies in anesthesia and critical care have shown success in improving patient outcomes and care standards, indicating that this approach is both valuable and tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients undergoing Anesthesia or Critical care * Signed informed consent. Exclusion Criteria: Refused informed consent
Where this trial is running
Milan, MI
- Ospedale San Raffaele di Milano — Milan, Mi, Italy (Recruiting)
Study contacts
- Study coordinator: Marina Pieri, MD
- Email: pieri.marina@hsr.it
- Phone: +39022643
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.