ClinicalTrials.gg
Status unknownNCT00425685Updated Jan 23, 2007

Use of ECMO in Acute MI

An observational study in ECMO and Acute MI, sponsored by Johann Wolfgang Goethe University Hospital. Status unknown. Open to participants aged 17 Years to 90 Years. Per ClinicalTrials.gov, last updated 2007-01-23.

Sponsored by Johann Wolfgang Goethe University Hospital · Observational

The sponsor has not verified this record recently (last verified Jan 2007), so the status shown — last known as Active, not recruiting — may be out of date.
Study type
Observational
Model
Defined population
Time perspective
Other
Enrollment
60
Ages
17 Years to 90 Years
Sex
All
01

Study summary

ECMO offers an acceptable cardiopulmonary support in adults with similar hospital survival rates as other mechanical support. It is versatile and salvages some patients, who may otherwise die. Improvement in intermediate term outcome will require multidisciplinary approach to protect organ function and limit organ injury during this support.

Read the detailed description

Extracorporeal membrane oxygenation (ECMO) is an established treatment option in patients with Cardiogenic Schock. We retrospectively reviewed early and mid-term outcome as well as predictors of survival during using ECMO. This report reviews our experience with this support system in last 3 years.

02

Conditions studied

  • ECMO and Acute MI

Keywords

  • cardiopulmonary resuscitation, ECMO, shock, survival, heart failure, transplantation, heart assist device.
03

In context

Shock

922 studies on the registry are indexed under Shock; 172 are open to participants now.

This study's enrollment of 60 is below the median of 93 across 355 observational studies indexed under Shock.

Browse Shock studies →

Lead sponsor

Johann Wolfgang Goethe University Hospital is the lead sponsor of 160 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
17 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Acute MI

Exclusion criteria

Exclusion Criteria:

  • Contraindication against ECMO
05

Study design

Observational model
Defined population
Time perspective
Other
Enrollment
60 participants
06

Study locations

No study locations are listed for this record.

07

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2003 and a completion of Dec 2006. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 22, 2007
First posted
Jan 23, 2007
Start
Jan 2003
Completion
Dec 2006
Last update
Jan 23, 2007
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
No changes since tracking began. The registry record was last updated on Jan 23, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00425685
First posted
Jan 23, 2007
Start date
Jan 2003
Completion
Dec 2006
Last update
Jan 23, 2007

Study contacts

Farhad Bakhtiary, MD
principal investigator · JW Goethe University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2007. You cannot join it, but the record below documents what was studied.

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