No registrations found.
ID
Source
Brief title
Health condition
Respiratory failure
Sponsors and support
Intervention
Outcome measures
Primary outcome
Primary Objective: Accessing weaning practices in VV-ECMO Care.
Secondary outcome
Secondary Objective(s): Accessing amount of ECMO runs, cannulation strategies, ventilation care during VV-ECMO support, targets in oxygenation and ventilation, sedation targets during VV-ECMO, accessing weaning failure, rate of referral due to weaning failure.
Background summary
Rationale: The process of weaning from VV-ECMO is being done in many different protocol’s, which mostly are not evidence based.
Objective: To access the process and choices that are made during the weaning from VV-ECMO in ECMO centres.
Study design: Prospective observational questionary study.
Study population: Medical (ICU) specialists involved in the management of ECMO patients at their hospital.
Intervention (if applicable): 1 (coordinating) medical specialist per ECMO hospital will receive a short questionnaire.
Main study parameters/endpoints: Description of choices made in the weaning process of VV-ECMO like minimally acceptable mechanical ventilation settings, settings of the ECMO machine, the way a ‘trial off ECMO’ is performed.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: There are no risk involved in participating in this questionnaire study.
Study objective
There are multiple ways of weaning from venovenous ECMO support
Study design
Primary objective: Answers to the questionairres which is sent to the participant will be collected at one time point, 4 weeks after sending the questionnaire. Depending on the type of question qualitative measure methods or averages, mean and standard deviations will be used to measure the outcome.
Secondary objective(s): Answers to the questionairres which is sent to the participant will be collected at one time point, 4 weeks after sending the questionnaire. Depending on the type of question qualitative measure methods or averages, mean and standard deviations will be used to measure the outcome.
Intervention
1 (coordinating) medical specialist per ECMO hospital will receive a short questionnaire.
Inclusion criteria
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- Intensivist responsible for ECMO care in ECMO centre who perform VV-ECMO on a regular basis.
Exclusion criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- More than one intensivist per hospital
- Subject works in a hospital without ECMO Care of who do not provide VV-ECMO Care.
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL9863 |
| Other | METC LUMC : Not available jet |