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iver stiffness in septic shock patients

Not Applicable
Conditions
Health Condition 1: I958- Other hypotension
Registration Number
CTRI/2023/06/053891
Lead Sponsor
Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Adult patients with septic shock, on vasopressor for at least 24 hours

AND

Documentation of normal LFT and normal echogenicity of liver on ultrasound during current illness (before inclusion)

Exclusion Criteria

1.Age <18 years

2.Onset of septic shock >7 days

3.Known liver disease (viral hepatitis, non-alcoholic fatty liver disease, alcoholic liver

4.disease, autoimmune, cholestasis and genetic liver disease, focal liver disease)

5.Congestive heart failure

6.BMI >35

7.Pregnancy

8.Intraabdominal hypertension

9.Recent history of abdominal trauma or surgery

10.Technical difficulties (breathe holding/unable to transport)

11.Patients who do not provide written consent

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study the prevalence & severity of increased liver stiffness in patients with septic shockTimepoint: Within 7 days of septic shock
Secondary Outcome Measures
NameTimeMethod
To study the change in liver stiffness, 4-6 weeks after stopping vasopressorsTimepoint: Within 6 weeks after ICU discharge
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