Viewing Study NCT04680663



Ignite Creation Date: 2024-05-06 @ 3:36 PM
Last Modification Date: 2024-10-26 @ 1:52 PM
Study NCT ID: NCT04680663
Status: COMPLETED
Last Update Posted: 2020-12-28
First Post: 2020-12-18

Brief Title: Predictor of Postoperative Complications After Lengthy Surgical Procedures
Sponsor: Cairo University
Organization: Cairo University

Study Overview

Official Title: Peripheral Perfusion Index Versus Serum Lactate Levels as Predictor of Postoperative Complications and Prolonged ICU Stay After Lengthy Surgical Procedures a Prospective Observational Study
Status: COMPLETED
Status Verified Date: 2024-07
Last Known Status: ENROLLING_BY_INVITATION
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Many patients undergoing long time surgery will manifest increased level of blood lactate

Hyperlactacidemia can cause disturbance of internal environment then leading to increased complications and longer ICU stay even death For postoperative patients we must ensure adequate perfusion in order to minimize the length of hyperglycemia and improve patients outcomes With regard to lactate it provides information about prefusion but not timely enough for its delay on reflecting hypoperfusion And its not real-time and non-invasive

Peripheral perfusion index PPI is an indicator reflecting hypoperfusion in critical patients It is measured using pulse co-oximetry technology which is characterized by being real-time and noninvasive PPI is defined as the ratio of pulsatile blood flow to the non-pulsatile blood flow mirroring the strength of blood flow and quality of perfusion at sensor site reflecting perfusion state of the body part In contrast to lactate value its real-time and easy to monitor
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None