Actively Recruiting

All Genders
Healthy Volunteers
ID06792773

2024 NewAnescat Register

Led by Consorci Sanitari de Terrassa · Updated on 2026-02-04

13634

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to assess the current work situation of anaesthesiology services in Spain, 20 years after the first comprehensive record called ANESCAT 2003. It evaluates whether the increase in healthcare activity matches the growth in resources allocated to the specialty and provides objective data for future planning and demands. The study focuses on collecting data on anaesthesia activities across several areas, including surgical procedures, intensive care units, chronic pain units, and delivery rooms. This data is gathered through various questionnaires covering a 14-day activity period over the course of one year. Participants will be involved by having their anaesthesia work activity recorded during this 14-day period. Researchers will measure the extent of anaesthesia services in different clinical settings and evaluate staff activity levels, as well as the role of anaesthesiology in managing polytrauma patients and cardiorespiratory arrest. The study spans one year to capture comprehensive activity data.

CONDITIONS

Brief Title

2024 NewAnescat Register

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Anaesthesiologists involved in clinical activities across various areas
  • Participation in anaesthesia work over a continuous 24-hour period
  • Willingness to complete questionnaires about anaesthesia activities
  • Availability to report work activity during a 14-day period within one year
  • Inclusion of all patients without restriction criteria
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote)

Monitoring

Duration - 14 days within one year

Participants report their anaesthesia work activity during a 14-day period within one year, including time spent across various clinical areas such as surgical activity, intensive care units, chronic pain units, and delivery rooms.

Daily activity reporting during the 14-day period

Trial Site Locations

Total: 1 location

1

Hospital Clinic de Barcelona

Barcelona, Barcelona, Spain, 08036

Actively Recruiting

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Research Team

C

Carles Espinós, MD

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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