Czech Anesthesia Day 2019 (CAD2019)

February 17, 2021 updated by: Petr Štourač, MD, Brno University Hospital

Czech Anesthesia Day 2019: Observational Trial

Czech Anesthesia Day 2019 was designed as a prospective observational trial with the aim to evaluate the current anesthesiology practice in Czech Republic.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

Anesthesiology centers in Czech Republic was screened for cooperation during the year 2018. Data from centers with previously confirmed cooperation will be screened and filled into the electronic database. The basic information about the centre, patient´s demography, American Society of Anesthesiologist classification (ASA), type of surgery/anesthesia, airway management, type of anesthesia induction, drugs for anesthesia induction a and anesthesia maintenance, used monitors of vital signs and functions, type and amount of infusions, temperature management, intravenous lines management, patient blood management, mechanical ventilation settings and postoperative admission will be recorded.

Study Type

Observational

Enrollment (Anticipated)

1000

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Czechia
      • Ústí Nad Labem, Czechia, 401 13
        • Krajska zdravotni a.s. University Hospital Usti nad Labem
    • South Moravian Region
      • Brno, South Moravian Region, Czechia, 62500
        • Brno University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • ADULT
  • OLDER_ADULT
  • CHILD

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients undergoing surgical or diagnostic procedure under anesthesia in the Czech Republic

Description

Inclusion Criteria:

  • Patients from confirmed Anesthesiology Centers - previously confirmed the cooperation (center is registered in the online database with the unique identification)

Exclusion Criteria:

  • Data from centers with not confirmed cooperation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients undergoing anesthesia in Czech Republic
Patients undergoing anesthesia in Czech Republic in the selected period from the confirmed Anesthesia Center
Other: Anesthesia
Patients undergoing anesthesia from the cooperating Anesthesia center

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anesthesia description
Time Frame: From anesthesia induction until the admission to postanesthesia care
Data from confirmed center will be recorded with the aim to describe the daily anesthesia practice in Czech Republic
From anesthesia induction until the admission to postanesthesia care

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Brno University Hospital

Collaborators

Krajská zdravotní a.s. University Hospital Ústí nad Labem

Investigators

  • Study Director: Vladimir Cerny, Prof.MD.Ph.D., Krajska zdravotni a.s. University Hospital Usti nad Labem

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

December 11, 2019

Primary Completion (ANTICIPATED)

June 30, 2021

Study Completion (ANTICIPATED)

December 31, 2021

Study Registration Dates

First Submitted

December 26, 2019

First Submitted That Met QC Criteria

December 26, 2019

First Posted (ACTUAL)

December 30, 2019

Study Record Updates

Last Update Posted (ACTUAL)

February 18, 2021

Last Update Submitted That Met QC Criteria

February 17, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • KDAR FN Brno 2019/12

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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