search
Back to results

Focused Ultrasound in Septic Shock Patients

Primary Purpose

Septic Shock

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
ultrasound examination
Ultrasound group
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Septic Shock focused on measuring critical ultrasound

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

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

Exclusion Criteria:

  • age < 18yr
  • pregnant
  • DNR

Sites / Locations

  • Peking Union Medical College Hospital ICURecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Rutine treatment group, Ultrasound group

Arm Description

Outcomes

Primary Outcome Measures

mortality

Secondary Outcome Measures

Full Information

First Posted
August 1, 2013
Last Updated
August 9, 2013
Sponsor
Peking Union Medical College Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT01920776
Brief Title
Focused Ultrasound in Septic Shock Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2013
Overall Recruitment Status
Unknown status
Study Start Date
July 2013 (undefined)
Primary Completion Date
July 2014 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking Union Medical College Hospital

4. Oversight

5. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock
Keywords
critical ultrasound

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rutine treatment group, Ultrasound group
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
ultrasound examination
Intervention Type
Other
Intervention Name(s)
Ultrasound group
Intervention Description
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.
Primary Outcome Measure Information:
Title
mortality
Time Frame
28day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age>18yr survive more than 24hrs fulfilled septic shock Exclusion Criteria: age < 18yr pregnant DNR
Facility Information:
Facility Name
Peking Union Medical College Hospital ICU
City
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaoting Wang, Doctor
Phone
86-10-69152300
Email
ozohom@yahoo.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
27411452
Citation
Du W, Wang XT, Long Y, Liu DW. Efficacy and Safety of Esmolol in Treatment of Patients with Septic Shock. Chin Med J (Engl). 2016 Jul 20;129(14):1658-65. doi: 10.4103/0366-6999.185856.
Results Reference
derived

Learn more about this trial

Focused Ultrasound in Septic Shock Patients

We'll reach out to this number within 24 hrs