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Trial record 1 of 1 for:    NCT01920776
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Focused Ultrasound in Septic Shock Patients

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ClinicalTrials.gov Identifier: NCT01920776
Recruitment Status : Unknown
Verified August 2013 by XIiaoting Wang, Peking Union Medical College Hospital.
Recruitment status was:  Recruiting
First Posted : August 12, 2013
Last Update Posted : August 12, 2013
Sponsor:
Information provided by (Responsible Party):

Study Description
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.

Condition or disease Intervention/treatment
Septic Shock Other: ultrasound examination Other: Ultrasound group

Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 100 participants
Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Study Start Date : July 2013
Estimated Primary Completion Date : July 2014

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Shock Ultrasound
U.S. FDA Resources

Arms and Interventions

Arm Intervention/treatment
Experimental: Rutine treatment group, Ultrasound group Other: ultrasound examination Other: 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.


Outcome Measures

Primary Outcome Measures :
  1. mortality [ Time Frame: 28day ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 70 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • age < 18yr
  • pregnant
  • DNR
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01920776


Locations
China
Peking Union Medical College Hospital ICU Recruiting
Beijing, China, 100730
Contact: Xiaoting Wang, Doctor    86-10-69152300    ozohom@yahoo.com   
Sponsors and Collaborators
Peking Union Medical College Hospital
More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: XIiaoting Wang, Dr, Peking Union Medical College Hospital
ClinicalTrials.gov Identifier: NCT01920776     History of Changes
Other Study ID Numbers: LHMBCSDXJS-SEPTIC SHOCK
First Posted: August 12, 2013    Key Record Dates
Last Update Posted: August 12, 2013
Last Verified: August 2013

Keywords provided by XIiaoting Wang, Peking Union Medical College Hospital:
critical ultrasound

Additional relevant MeSH terms:
Shock
Shock, Septic
Pathologic Processes
Sepsis
Infection
Systemic Inflammatory Response Syndrome
Inflammation