NCT04188886

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2019

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2019

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

October 29, 2019

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 29, 2019

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 6, 2019

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2020

Completed
Last Updated

December 6, 2019

Status Verified

December 1, 2019

Enrollment Period

8 months

First QC Date

October 29, 2019

Last Update Submit

December 5, 2019

Conditions

Outcome Measures

Primary Outcomes (1)

  • Evaluation the involvement of professionals in ECMO-related decisions

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

    1 day

Secondary Outcomes (4)

  • 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

Interventions

Practice survey on

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Bourgogne Franche Comté

Dijon, 21000, France

RECRUITING

Central Study Contacts

Aline LAUBRIET JAZAYERI, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PI

Study Record Dates

First Submitted

October 29, 2019

First Posted

December 6, 2019

Study Start

March 1, 2019

Primary Completion

October 29, 2019

Study Completion

December 31, 2020

Last Updated

December 6, 2019

Record last verified: 2019-12

Data Sharing

IPD Sharing
Will not share

The data will not be disclosed individually to other researchers. The analysis is done in a global way

Locations