Viewing Study NCT05792696



Ignite Creation Date: 2024-05-06 @ 6:48 PM
Last Modification Date: 2024-10-26 @ 2:55 PM
Study NCT ID: NCT05792696
Status: RECRUITING
Last Update Posted: 2024-01-03
First Post: 2023-03-19

Brief Title: PPI Guided Strategies for Prevention and Treatment of Intraoperative Hypotension
Sponsor: zhiqiang zhou
Organization: Tongji Hospital

Study Overview

Official Title: Effectiveness of Peripheral Perfusion Index Guided Strategies for the Prevention and Treatment of Hypotension a Randomized Trial
Status: RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
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: Intraoperative hypotension is closely related to the poor prognosis of surgery The study is focused on the effectiveness of maintaining normal peripheral perfusion index PPI on time-weighted average of hypotension during anesthesia
Detailed Description: Intraoperative hypotension is closely related to the poor prognosis of surgery Hypotension decreased blood flow perfusion of organs which lead to dysfunction of multiple organs especially increasing serious complications such as cardio-cerebrovascular events and acute renal injury within 30 days after surgery The aim of this study is to establish a set of strategies that can effectively prevent and treat intraoperative hypotension so as to alleviate possible harm to patients from perioperative hypotension The study is focused on the effectiveness of maintaining normal peripheral perfusion index PPI on time-weighted average of hypotension during anesthesia The lower target mean arterial pressure MAP was higher than 65 mmHg MAP less than 65 mmHg was defined as intraoperative hypotension between induction and tracheal extubation

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