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NCT01685112 Clinical Trial

Comparison of ECMO Use and Conventional Treatment in Adults With Septic Shock

Septic Shock Clinical Trial

Official title:
Comparison of ECMO Use and Conventional Treatment in Adults With Septic Shock

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01685112
Other study ID # 201207079RIC
Secondary ID
Status Recruiting
Phase N/A
First received September 11, 2012
Last updated October 10, 2012
Start date September 2012
Est. completion date August 2013

Study information
Verified date September 2012
Source National Taiwan University Hospital
Contact YuChung Chuang, MD
Phone 886-972652532
Email weischuang@gmail.com
Is FDA regulated No
Health authority Taiwan: Department of Health
Study type Observational

Clinical Trial Summary

Although few cases reported successful treatment of septic shock using extracorporeal membrane oxygenation (ECMO) in adults, no studies compared ECMO to conventional treatment (without ECMO) as treatment for adults with septic shock. Since it is difficult to conduct a randomized study to allocate patients in such critical condition, we aimed to conduct a retrospective observational study using propensity score matched analysis to compare the survival of adults with septic shock treated by ECMO or conventional treatment.

Recruitment information / eligibility
Status Recruiting
Enrollment 300
Est. completion date August 2013
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- age >20

- admitted at ICU

- septic shock

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
Taiwan National Taiwan University Hospital Taipei

Sponsors (1)
Lead Sponsor Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary In hospital mortality inhospital mortality as primary outcome, mean length of hospital stay around 30 days 30 days No
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