Anesthesia PracticeCAD2019NCT04213495
Czech Anesthesia Day 2019
An observational study of Anesthesia Practice, run by Brno University Hospital at 2 sites in Czechia.
Trial summary
Czech Anesthesia Day 2019 was designed as a prospective observational trial with the aim to evaluate the current anesthesiology practice in Czech Republic. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Anesthesia Practice
- What is being tested?
- Anesthesia
- How many people
- 1,000 participants
- Where
- 2 sitesCzechia
- Study dates
- 11 Dec 2019to 31 Dec 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- Child, Adult, Older adult
Study population: Patients undergoing surgical or diagnostic procedure under anesthesia in the Czech Republic
Who may be able to join
- Patients from confirmed Anesthesiology Centers - previously confirmed the cooperation (center is registered in the online database with the unique identification)
Who cannot join
- Data from centers with not confirmed cooperation
Trial locations and contacts
2 sites in 1 country.
Czechia2 sites
Brno University Hospital
Brno, South Moravian, 62500
Krajska zdravotni a.s. University Hospital Usti nad Labem
Ústí nad Labem, 401 13
About this study
Official title: 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.
Read the 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.
- Conditions
- Anesthesia Practice
- Being tested
- Anesthesia
- Keywords
- Anesthesia, Practice, Czech Republic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
AnesthesiaOther
Patients undergoing anesthesia from the cooperating Anesthesia center
| Study group | Role | What they receive |
|---|---|---|
| Patients undergoing anesthesia in Czech Republic | Patients undergoing anesthesia in Czech Republic in the selected period from the confirmed Anesthesia Center Receives: Other: Anesthesia |
What is being measured
The primary outcome is the main question the study is designed to answer.
Anesthesia description
Data from confirmed center will be recorded with the aim to describe the daily anesthesia practice in Czech Republic
Measured: From anesthesia induction until the admission to postanesthesia care
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Dec 2019
- Study start11 Dec 2019
- Primary completion30 Jun 2021 (estimated)
- Study completion31 Dec 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Anesthesia PracticeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Brno University Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- Krajská zdravotní a.s. University Hospital Ústí nad Labem
- Responsible party
- Principal investigator, Petr Štourač, MD, Brno University Hospital
- Investigators
- Petr Stourac, assoc.Prof.MD.Ph.D, Study chair, Brno University HospitalVladimir Cerny, Prof.MD.Ph.D., Study director, Krajska zdravotni a.s. University Hospital Usti nad Labem
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04213495
- Sponsor's protocol ID
- KDAR FN Brno 2019/12
- Acronym
- CAD2019
- Status last verified
- Feb 2021
- First submitted
- 26 Dec 2019
- Last updated
- 18 Feb 2021
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 18 Feb 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Czech Anesthesia Day 2019: Observational Trial
- ClinicalTrials.gov ID
- NCT04213495
- Acronym / sponsor ID
- CAD2019 / KDAR FN Brno 2019/12
- Conditions
- Anesthesia Practice
- Keywords
- Anesthesia, Practice, Czech Republic
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- Brno University HospitalUniversity, hospital or other
- Collaborators
- Krajská zdravotní a.s. University Hospital Ústí nad Labem
- Study start
- 11 Dec 2019 (actual)
- Primary completion
- 30 Jun 2021 (estimated)
- Study completion
- 31 Dec 2021 (estimated)
- First posted
- 30 Dec 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Czech Anesthesia Day 2019 was designed as a prospective observational trial with the aim to evaluate the current anesthesiology practice in Czech Republic.
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 design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients undergoing anesthesia in Czech Republic | – | Other: AnesthesiaPatients undergoing anesthesia in Czech Republic in the selected period from the confirmed Anesthesia Center |
Who may qualify
- Sex
- All
- Age groups
- Child, Adult, Older adult
- Study population
- Patients undergoing surgical or diagnostic procedure under anesthesia in the Czech Republic
Key inclusion criteria (1 listed)
- Patients from confirmed Anesthesiology Centers - previously confirmed the cooperation (center is registered in the online database with the unique identification)
Key exclusion criteria (1 listed)
- Data from centers with not confirmed cooperation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| AnesthesiaPatients undergoing anesthesia from the cooperating Anesthesia center | Other | Patients undergoing anesthesia in Czech Republic |
Primary outcome
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
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Feb 2021.
- Individual participant dataSharing planned: Undecided
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Anesthesia
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Petr Stourac, assoc.Prof.MD.Ph.D study chair
Brno University Hospital
Vladimir Cerny, Prof.MD.Ph.D. study director
Krajska zdravotni a.s. University Hospital Usti nad Labem
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Anesthesia Practice, run by Brno University Hospital at 2 sites in Czechia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 18 Feb 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Czechia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Anesthesia description (time frame: From anesthesia induction until the admission to postanesthesia care). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Feb 2021.