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NCT01920776 Clinical Trial

Focused Ultrasound in Septic Shock Patients

Septic Shock Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01920776
Other study ID # LHMBCSDXJS-SEPTIC SHOCK
Secondary ID
Status Recruiting
Phase N/A
First received August 1, 2013
Last updated August 9, 2013
Start date July 2013

Study information
Verified date August 2013
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority National Health and Family Planning Commission of People's Republic of China : China
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that lung ultrasound and echocardiography will benefit the septic shock patients by making the treatment more precisely and rapidly. Septic shock patients from multicenter will be enrolled in the study. They will be randomly divided into two groups. The routine treatment group will receive routine treatment according to the SSC guideline. The study group will receive additional ultrasound examination, which will decide the improvement of therapy. Therapy change based on ultrasound results and the prognosis will be recorded.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date
Est. primary completion date July 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- age>18yr

- survive more than 24hrs

- fulfilled septic shock

Exclusion Criteria:

- age < 18yr

- pregnant

- DNR

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Other:
• ultrasound examination

• Ultrasound group
Ultrasound group will receive ultrasound examination at least once a day, the results will be noted to the attending who is in charge of the treatment.

Locations
Country Name City State
China Peking Union Medical College Hospital ICU Beijing

Sponsors (1)
Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary mortality 28day Yes
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