NCT02837419

Brief Summary

This study evaluates patients on ECLS treatment as considered appropriate with mortality and health related Quality of life and costs.

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
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Dec 2017

Typical duration for all trials

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

First Submitted

Initial submission to the registry

July 15, 2016

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 19, 2016

Completed
1.4 years until next milestone

Study Start

First participant enrolled

December 1, 2017

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2020

Completed
Last Updated

September 25, 2019

Status Verified

September 1, 2019

Enrollment Period

2.1 years

First QC Date

July 15, 2016

Last Update Submit

September 24, 2019

Conditions

Keywords

extracorporeal life supporthealth related quality of life

Outcome Measures

Primary Outcomes (1)

  • health related quality of life

    health related quality of life with EQ-5D questionnaire at 6 and 12 months

    12 months

Interventions

Quality of Care

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Critically ill patients on the ICU treated with extracorporeal life support

You may qualify if:

  • Admitted to intensive care
  • Treated with extracorporeal life support

You may not qualify if:

  • none

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Medical Center Groningen

Groningen, 9700 RB, Netherlands

RECRUITING

Related Publications (2)

  • Jolink FEJ, Onrust M, Dos Reis Miranda D, Mandigers L, Delnoij T, Maas JJ, Raasveld SJ, Vlaar APJ, Donker DW, Scholten E, de Metz J, van den Brule J, Kuijpers M, Vermeulen KM, van der Voort PHJ, van den Bergh WM, Oude Lansink-Hartgring A; Dutch Extracorporeal Life Support (ECLS) Study Group. Five Years After Extracorporeal Membrane Oxygenation: A Prospective Cohort Study of Health-Related Quality of Life and Patient Outcomes. Crit Care Med. 2025 Dec 1;53(12):e2487-e2496. doi: 10.1097/CCM.0000000000006900. Epub 2025 Oct 15.

  • Oude Lansink-Hartgring A, Dos Reis Miranda D, Donker DW, Maas JJ, Delnoij T, Kuijpers M, van den Brule J, Scholten E, Endeman H, Vlaar APJ, van den Bergh WM; Dutch ECLS study group. Cost-effectiveness in extracorporeal life support in critically ill adults in the Netherlands. BMC Health Serv Res. 2018 Mar 9;18(1):172. doi: 10.1186/s12913-018-2964-6.

MeSH Terms

Conditions

Critical Illness

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • walter m van den Bergh, MD, PhD

    department of critical care, UMCG

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Wim Dieperink, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
12 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
research coordinator

Study Record Dates

First Submitted

July 15, 2016

First Posted

July 19, 2016

Study Start

December 1, 2017

Primary Completion

January 1, 2020

Study Completion

January 1, 2020

Last Updated

September 25, 2019

Record last verified: 2019-09

Locations