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NCT Number: NCT06758908

Prevelance, Predictors and Outcome of Sepsis Associated Liver Injury (SALI)

prevelance, predictors and outcome of sepsis associated liver injury (SALI)

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Key information

Conditions

Liver Injuries

Age range

15 year–75 year

Sex eligibility

All sexes

Study type

Observational

About this study

patient with liver disease and sepsis at the same time

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • clinical diagnosis of SALI
  • must take liver support

Exclusion criteria

  • SALI
  • Thyroid disease

Treatment and study plan

Antibiotic

Device

SALI

Primary outcomes

  1. prevelance, predictors and outcome of sepsis associated liver injury (SALI)

    Time frame: baseline

    analysis outcome of sepsis associated liver injury (SALI)

  2. 28 days mortality

    Time frame: baseline

    patient with liver dieases and sepsis

  3. patient shouldn't be in pain

    Time frame: baseline

    patient in study not in pain

Secondary outcomes

  1. patient stay in hospital 2weeks

    Time frame: baseline

    patient with liver dieases and sepsis

Study contacts

Contact information is provided by the study sponsor or research team.

Dinal ali hamad dina hamad, specialist

CONTACT

[email protected]

01063040703

Mahmoud sayed zohry, first mastar

CONTACT

[email protected]

01225463889 ext. 01069209843

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Collaborators

  • Investigator

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jan 6, 2025
Registry last updated
Jan 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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