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Clinical Trial Summary

To identified prevalence, risk factors, and prognostic factors of IAH and ACS in surgical critically ill patients in institutional hospital


Clinical Trial Description

Every postoperative patients admitted to surgical ICU who meet inclusion criteria will be asked for informed consent. After obtained, intraabdominal pressure (IAP) will be measured through already placed Foley's catheter simultaneously with patients's data record. If patients don't have IAH or ICS, IAP will be measured daily until discharge from ICU or removal of Foley's catheter. If patients have IAH or ACS, IAP will be measured every 6-8 hours until IAP is less than 12 mmHg then it will be measures daily until discharge from ICU or removal of Foley's catheter. After completion of data collection, data will be analyzed accordingly. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03762057
Study type Observational [Patient Registry]
Source Ramathibodi Hospital
Contact Cherdkiat Karnjanarachata, MD
Phone +66-85-5774747
Email chird_na@yahoo.com
Status Not yet recruiting
Phase
Start date December 10, 2018
Completion date June 10, 2020

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