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Clinical Trials/NCT04188886
NCT04188886
Unknown
Not Applicable

Evaluation of the Daily Practices of ECMO Veino-arterial and Their Ethical Implications in France: Multicenter Observational Study (Evaluation of Professional Practice)

Centre Hospitalier La Chartreuse1 site in 1 country500 target enrollmentMarch 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Life Support Systems
Sponsor
Centre Hospitalier La Chartreuse
Enrollment
500
Locations
1
Primary Endpoint
Evaluation the involvement of professionals in ECMO-related decisions
Last Updated
6 years ago

Overview

Brief Summary

Short-term circulatory support (ECMO/ECLS) has become a common emergency resuscitation support.

Currently, the indication of the ECMO/ECLS relies more on clinic, biological and imagery arguments than on a real consensus.During the care of a patient under ECMO/ECLS, various stakeholders are involved in the implementation and its medical and paramedical management. Everyone, with their knowledge and experience, has an opinion on the relevance of this therapy.

Detailed Description

A validated questionnaire, translated from an Anglo-Saxon study, will be used as a basis for work and adapted. After the publication of a memo, it is accessible anonymously on a platform (ASKABOX) whose link is distributed by email by the secretaries or nursing staff. The city and the exercise service will be requested in the preamble of the questionnaire. It is composed of six demographic questions: age, gender, occupation, participation in emergency care, number of ECMOs encountered, level of knowledge about ECMO. The other questions concern concrete ECMO situations and the answers are nuanced from definitely yes to definitely no to allow professionals to express their opinion as well as possible. The targeted professionals are all those involved in the management of patients on ECMO: emergency physicians, anesthesiologists, surgeons, perfusionists, nurses, orderlies, ASHs. A monocentric feasibility study was carried out with satisfactory results in terms of participation. AN INFORMATION NOTE WILL BE ATTACHED WITH THE EMAIL AND THE LINK FOR THE QUESTIONNAIRE (ANONYMOUS)

Registry
clinicaltrials.gov
Start Date
March 1, 2019
End Date
December 31, 2020
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Centre Hospitalier La Chartreuse
Responsible Party
Principal Investigator
Principal Investigator

MORGANT Marie-Catherine

PI

Centre Hospitalier La Chartreuse

Eligibility Criteria

Inclusion Criteria

  • All medical and paramedical personnel involved in decision making, installation, and monitoring of the ECMO

Exclusion Criteria

  • MEDICAL AND PARAMEDICAL STAFF NOT INVOLVED IN THE ESTABLISHMENT OR FOLLOW-UP OF THE ECMO

Outcomes

Primary Outcomes

Evaluation the involvement of professionals in ECMO-related decisions

Time Frame: 1 day

Through an anonymous questionnaire, the investigators will evaluate the speciality (eg cardiac surgeon, anesthesiologist...) of the doctor responsible for the indication of ECLS

Secondary Outcomes

  • Identification of the profession of each person involved in the management of the patients(1 day)
  • Demographic data (age, sexe) of each personnel involved in the management of the patients(1 day)
  • Level of training and knowledge of each personnel involved in the management of the patients(1 day)
  • Opinion of the health care staff on the care management of the patients(1 day)

Study Sites (1)

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