Detection of Health Risk Situations in the Anesthesia Consultation.
1 other identifier
observational
218
1 country
1
Brief Summary
This study aims to estimate the proportion of patients seen in the anesthesiology consultation for planned surgery in whom a previously unknown health risk situation is detected (e.g., obesity, anemia, etc.).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 5, 2024
CompletedFirst Posted
Study publicly available on registry
December 9, 2024
CompletedStudy Start
First participant enrolled
February 4, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedFebruary 12, 2025
February 1, 2025
10 months
December 5, 2024
February 10, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
unknown health risk situation
proportion of patients with a unknown health risk situation
1 year
Interventions
a unknown health risk situation detected at anestesiology consult
Eligibility Criteria
Patients evaluated in person at the preoperative anesthesia consultation for a scheduled surgery indication.
You may qualify if:
- Men and women aged 18 to 50 years.
- Indication for elective surgery.
- In-person preoperative evaluation in the scheduled Anesthesiology consultation.
You may not qualify if:
- Indication for non-deferrable urgent surgery.
- Pregnant women.
- Pre-surgical visit outside the anesthesia consultation.
- Incomplete preoperative evaluation, as indicated in the final section (preoperative judgment) of the anesthesia visit report.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Consorci Sanitari Alt Penedés-Garraf
Vilafranca Del Penedés, Barcelona, Spain
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 5, 2024
First Posted
December 9, 2024
Study Start
February 4, 2025
Primary Completion
December 1, 2025
Study Completion
December 1, 2025
Last Updated
February 12, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- After publication of main results of the study.
- Access Criteria
- IPD will be shared only for scientific research purposes and following the Spanish and European Union normative law about data protection. The requirements will be directed to the IP of the study. The IP will evaluate the request to verify and evaluate the data that is requested and the purposes for which it is requested. Next, the IP will transfer the request to the promotor center the study for the final decision.
IPD (without personal identification data) could be shared by requirement from other researchers after the end of the study, and only for research purposes and previous approval of promotor center of the study (CSAPG). Anyway, Spanish and European Union legal policy about data protection will strictly be followed (IPD will not be transferred outside European Union).