2024 NewAnescat Register

NCT06792773 | Recruiting

• 1 other identifier: PI-23-280
• Study Type: observational
• Target: 13,634
• Locations: 1 country
• Sites: 1

Brief Summary

20 years ago, for the first time in Spain, a record was made of all the activity carried out by a medical speciality, called ANESCAT 2003. After 20 years, the increase in healthcare activity has exceeded the expectations and predictions that were made at the time. Therefore, it is necessary to make a new assessment of the work situation in which our speciality finds itself in order to be able to evaluate whether the increase in resources allocated has been proportional and therefore to be able to have objective data with a view to making new demands and planning future needs.

Conditions

Anesthesia

Outcome Measures

Primary Outcomes (4)

• Anaesthesia surgical activity

  The main outcome and objective of the study is to quantify all the anaesthesia activity

  Assessed during the 14-day cut-off period of the study over one year

• Anaesthesia activity in the Intensive Care Units

  The main outcome and objective of the study is to quantify all the anaesthesia activity

  Assessed during the 14-day cut-off period of the study over one year

• Anaesthesia activity in the Chronic Pain Units

  The main outcome and objective of the study is to quantify all the anaesthesia activity

  Assessed during the 14-day cut-off period of the study over one year

• Anaesthesia activity in the delivery rooms

  The main outcome and objective of the study is to quantify all the anaesthesia activity

  Assessed during the 14-day cut-off period of the study over one year

Secondary Outcomes (3)

• Percentage of active staff in anaesthesiology services

  Assessed during the 14-day cut-off period of the study over one year

• The role of anaesthesiology services in Catalonia with regard to polytrauma patients

  Assessed during the 14-day cut-off period of the study over one year

• The role of anaesthesiology services in Catalonia with regard to cardiorespiratory arrest

  Assessed during the 14-day cut-off period of the study over one year

Eligibility Criteria

• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

The study population is all patients involving anaesthetic activity during the study days (14 days in a year).

The activity of all the areas in which the anaesthesiologist has some kind of work involvement over 24 hours during 14 days in a year is included through several questionnaires with different formats. Therefore all patients will be included without restriction criteria.

Contact the study team to discuss eligibility requirements. They can help determine if this study is right for you.

Sponsors & Collaborators

• Consorci Sanitari de Terrassa: lead

Study Sites (1)

Hospital Clinic de Barcelona

Barcelona, Barcelona, 08036, Spain

RECRUITING

Study Officials

• Carles Espinós, MD

  Germans Trias i Pujol Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Carles Espinós, MD

CONTACT

650125113; md071683@uic.es

Study Design

• Study Type: observational
• Observational Model: ECOLOGIC OR COMMUNITY
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Medical Doctor

Study Record Dates

• First Submitted: January 20, 2025
• First Posted: January 27, 2025
• Study Start: May 4, 2025
• Primary Completion: May 1, 2026
• Study Completion: May 1, 2026
• Last Updated: February 4, 2026

Record last verified: 2026-02

Locations

ES (1)