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Postoperative Gastrointestinal Dysfunction After High Risk Surgery

Surgery Clinical Trial

Official title:
Postoperative Gastrointestinal Dysfunction After High Risk Surgery: A Prospective Study in Adult Intensive Care Unit

Clinical Trial Summary

This study aims to find out the role of plasma I-FABP level, SOFA score, fluid balance, and vasopressor dose in predicting gastrointestinal dysfunction in high-risk postoperative patients treated in ICU

Clinical Trial Description

This is a prospective cohort study to find out the role of plasma I-FABP level, SOFA score, fluid balance, and vasopressor dose in predicting gastrointestinal dysfunction in high-risk postoperative patients treated in ICU. The characteristics of patients who meet the eligibility criteria were obtained. Blood sampling during admission is done for I-FABP level measurement and will be repeated after 24 hours. Blood sample which is not directly processed will be stored in refrigerator under 6-8C temperature. Evaluation of Acute Gastrointestinal Injury signs and symptoms is done. The re-evaluation is performed every day. If patients experiencing AGI signs and symptoms, monitoring and treatment based on condition are done. Routine follow-up is continued during hospitalisation in ICU. After all sample are collected, I-FABP level is assessed quantitatively using ELISA. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05867043
Study type Observational
Source Indonesia University
Contact Aldy Heriwardito, MD
Phone 3143336
Email aldy.heriwardito@gmail.com
Status Recruiting
Phase
Start date January 23, 2023
Completion date December 31, 2023
View Details
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