Anesthesia and Critical Care Registry
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversità Vita-Salute San Raffaele
About this trial
In recent decades, knowledge in the anesthesiology field has increasingly expanded, allowing for the refinement of monitoring techniques, therapies, and local-regional anesthesia maneuvers, and for the extension of care to a larger number of patients, including those previously excluded due to advanced age or comorbidities. Similarly, Intensive care management has continuously evolved, following innovations in the field of drugs and with the great diffusion of extracorporeal supports. The fundamental importance of registry studies has been recognized in this context to rapidly generate reliable data and improve the quality of care.
This prospective observational study is aimed at collecting data of all patients (expected 300,000) undergoing anesthesia or intensive care maneuvers at our institution. This registry aims to assist in carrying out registry-based clinical studies focused on improving current therapeutic and patient management standards.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients undergoing Anesthesia or Critical care
Signed informed consent.
Disqualifiers
None
Trial population
Any patients undergoing Anesthesia or critical care -related maneuvers admitted to our hospital. All patients will follow their normal course of diagnosis/treatment without any further requirements for the scope of this study other than those provided in the normal management of patients with this condition. Furthermore, any decision regarding drug or procedure will be made by the physician based on her/his clinical judgment in the context of clinical practice, independently from the decision to include the patient in this study. No follow-up medical and/or imaging examinations/laboratory analysis after hospital discharge are needed by the present study design.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Normal Clinical practice
Procedure/SurgeryNormal Clinical practice
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Clinical outcomes of patients urdergoing anesthesia and/or critical care
This study will collect data on the anesthesia-related and hospital outcome of patients undergoing anesthesia and intensive care. Due to the large sample size and heterogeneity of populations, further analysis will be planned to address homogenenous subgroups of patients.
Time frame
hospital discharge (usually <=30 days)Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov