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Clinical trial information and results are updated daily from ClinicalTrials.gov. The latest data update was conducted on 01/27/2021.

Survey of Regional Anesthesia Practice in Poland

Clinicaltrials.gov identifier NCT03923751

Recruitment Status Completed

First Posted April 23, 2019

Last update posted July 10, 2020

Study Description

Brief summary:

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.

  • Condition or Disease:Anesthesia, Regional
  • Intervention/Treatment: Other: Invitation to regional anesthesia survey
  • Phase: N/A
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 Design
  • Study Type: Observational
  • Actual Enrollment: 700 participants
  • Observational Model: Cohort
  • Time Perspective: Retrospective
  • Official Title: Survey of Regional Anesthesia Practice in Poland - National Survey 2018
  • Actual Study Start Date: May 2019
  • Actual Primary Completion Date: March 2020
  • Actual Study Completion Date: June 2020
Groups and Cohorts
Groups/Cohorts 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
Outcome Measures
  • Primary Outcome Measures: 1. 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
  • 2. 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
Eligibility Criteria
  • Ages Eligible for Study: (Child, Adult, Older Adult)
  • Sexes Eligible for Study: All
  • Accepts Healthy Volunteers: No
  • Sampling Method: Non-Probability Sample
  • Study Population: Anesthetists in Polish Hospitals
Criteria

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

Contacts and Locations
Contacts
Locations

Poland, Mazowieckie
I Department of Anesthesiology and Intensive Care Warsaw Medical University
Warsaw

Sponsors and Collaborators

Medical University of Warsaw

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)

More Information
  • Responsible Party: Medical University of Warsaw
  • ClinicalTrials.gov Identifier: NCT03923751 History of Changes
  • Other Study ID Numbers: Ankieta RA 2018
  • First Posted: April 23, 2019 Key Record Dates
  • Last Update Posted: July 10, 2020
  • Last Verified: July 2020
  • Individual Participant
    Data (IPD) Sharing
    Statement:
  • Plan to Share IPD: No
  • Plan Description: Results will be published only as collective data
  • Studies a U.S. FDA-regulated Drug Product: No
  • Studies a U.S. FDA-regulated Device Product: No