Actively Recruiting
Detection of Health Risk Situations in the Anesthesia Consultation
Led by Consorci Sanitari de l'Alt Penedès i Garraf · Updated on 2025-02-12
218
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are observing patients undergoing planned surgery to find out how often previously unknown health risks, like obesity or anemia, are identified during the anesthesiology consultation before surgery. The purpose is to estimate the proportion of patients with such hidden health issues detected at this evaluation. This observational study is sponsored by Consorci Sanitari de l'Alt Pened e8s i Garraf and focuses on adults aged 18 to 50 who are scheduled for elective surgery. The study involves an in-person preoperative evaluation during the scheduled anesthesiology consultation. Researchers will monitor whether any unknown health risk situations are discovered at this visit. There are no experimental treatments or interventions; instead, the study observes the natural findings during routine anesthesia consultations for surgery preparation. Participants will attend their usual anesthesiology consultation and undergo standard preoperative assessments. Researchers will record any newly found health risks during this visit. The primary measure is the detection of unknown health risk situations within one year. Participants' usual medical care continues without alteration, and the study aims to improve understanding of hidden health risks in surgical patients.
CONDITIONS
Brief Title
Detection of Health Risk Situations in the Anesthesia Consultation.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men and women aged 18 to 50 years
- Indication for elective surgery
- In-person preoperative evaluation in the scheduled Anesthesiology consultation
You will not qualify if you...
- Indication for non-deferrable urgent surgery
- Pregnant women
- Pre-surgical visit outside the anesthesia consultation
- Incomplete preoperative evaluation as noted in the anesthesia visit report
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 day
Participants undergo an in-person preoperative evaluation during the scheduled Anesthesiology consultation to detect any unknown health risk situations.
1 visit (in-person)
Duration - 1 year
Participants are observed over 1 year to monitor for any health risk situations detected during the anesthesia consultation.
Visits as per routine clinical care; no additional study visits required
Trial Site Locations
Total: 1 location
1
Consorci Sanitari Alt Penedés-Garraf
Vilafranca Del Penedés, Barcelona, Spain
Actively Recruiting
Research Team
L
Laura Mingüell, MD
N
Noemí Casaponsa
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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