Focused Ultrasound in Septic Shock Patients

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01920776

Enrollment

100

Registered

2013-08-12

Start date

2013-07-31

Completion date

Unknown

Last updated

2013-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Septic Shock

Keywords

critical ultrasound

Brief 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.

Interventions

OTHERultrasound examination

OTHERUltrasound 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.

Study design

Allocation

RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 70 Years

Healthy volunteers

Inclusion criteria

* age\>18yr * survive more than 24hrs * fulfilled septic shock

Exclusion criteria

* age \< 18yr * pregnant * DNR

Design outcomes

Primary

Measure	Time frame
mortality	28day

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026