Viewing Study NCT06586333



Ignite Creation Date: 2024-10-25 @ 8:02 PM
Last Modification Date: 2024-10-26 @ 3:39 PM
Study NCT ID: NCT06586333
Status: COMPLETED
Last Update Posted: None
First Post: 2024-09-04

Brief Title: Optimizing Stress Ulcer Prophylaxis Practices and Reducing Associated Costs in Intensive Care Units a Nonrandomized Controlled Study
Sponsor: None
Organization: None

Study Overview

Official Title: Evaluation of the Effect of an Education Program on Reducing the Efficacy and Costs of Inappropriate Stress Ulcer Prophylaxis in Intensive Care Units
Status: COMPLETED
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study is a prospectively designed nonrandomized controlled study It was conducted for six months at the EICU and GICU of a training and research hospital between 1 Jun 2023 and 1 December 2023
Detailed Description: The study involved GICU patients as the standard care services observation group OG The use of SUP in the GICU was only monitored and noted In the EICU patients were identified as part of the recruiting guideline group GG and in addition to receiving usual care they were managed for SUP according to the ASHP SUP guidelines 1 The study duration was six months concurrently in the EICU and the GICU Before inclusion written informed consent was obtained from each patient or their parentslegal guardians Subjects with incomplete data were excluded The inclusion criteria were patients aged 18 years and hospitalized for 24 hours in the EICUGICU Patients with a history of stomach cancer admission to the ICU because of GI bleeding subtotaltotal gastrectomy or receiving a proton pump inhibitor for therapeutic purposes were excluded from the study

Study Oversight

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