Survey of Regional Anesthesia Practice in Poland (AnkietaRA)

July 9, 2020 updated by: Marek Janiak, Medical University of Warsaw

Survey of Regional Anesthesia Practice in Poland - National Survey 2018

The study is being conducted to gain insight into regional anesthesia practice in polish hospitals specifically asking for methods used, accessibility to equipment and preference for regional blockade and perioperative analgesia.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

In recent years, regional anesthesia has become one of the most dynamic parts of anesthesiology. This is in part due to less invasive surgical procedures, surgical enhanced recovery protocols as well as the incorporation of ultrasonography into the daily practice of regional anesthesia.

The aim of this retrospective survey is to track and analyse the changes in everyday practice of regional anesthesia in Poland that have occurred in the year 2018.

An invitation to the survey will be sent to all heads of anesthesiology departments in Poland. The answers to the survey will be collected using an internet based website created by the authors of the study.

Study Type

Observational

Enrollment (Actual)

700

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

  • Poland
    • Mazowieckie
      • Warsaw, Mazowieckie, Poland, 02-005
        • I Department of Anesthesiology and Intensive Care Warsaw Medical University

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

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Anesthetists in Polish Hospitals

Description

Inclusion Criteria:

  • All Polish hospitals practising anesthesiology and intensive care in the national register of medical practices (www.rpwdl.csioz.gov.pl)

Exclusion Criteria:

  • Hospitals and medical practices not practising anesthesiology or intensive care

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
Polish Hospitals
Hospitals with anesthesia or intensive care practices
Other: Invitation to regional anesthesia survey
An invitation letter sent to Head of Anesthesiology and Intensive Care Department of Polish Hospital

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Regional anesthesia practice
Time Frame: Up to 12 months practice in the year 2018
Answers of head of anesthesiology and intensive care departments regarding regional anesthesia practice in their respective department by completing the Regional Anesthesia Survey 2018: multiple and single choice answers
Up to 12 months practice in the year 2018
Regional anesthesia practitioners
Time Frame: Up to 12 months in the year 2018
Answers of head of anesthesiology and intensive care departments regarding number of anesthesiologists practicing regional anesthesia
Up to 12 months in the year 2018

Collaborators and Investigators

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

Sponsor

Medical University of Warsaw

Collaborators

Department of Anesthesiology and Intensive Care, Czerniakowski Hospital, Warsaw
Polskie Towarzystwo Znieczulenia Regionalnego i Leczenia Bólu (Polish ESRA)
Sekcja Znieczulenia Regionalnego i Terapii Bólu, Polskie Towarzystwo Anestezjologii i Intensywnej Terapii (PTAiIT)

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)

May 21, 2019

Primary Completion (ACTUAL)

March 31, 2020

Study Completion (ACTUAL)

June 30, 2020

Study Registration Dates

First Submitted

April 18, 2019

First Submitted That Met QC Criteria

April 18, 2019

First Posted (ACTUAL)

April 23, 2019

Study Record Updates

Last Update Posted (ACTUAL)

July 10, 2020

Last Update Submitted That Met QC Criteria

July 9, 2020

Last Verified

July 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Ankieta RA 2018

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Results will be published only as collective data

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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