Viewing Study NCT04875390



Ignite Creation Date: 2024-05-06 @ 4:07 PM
Last Modification Date: 2024-10-26 @ 2:04 PM
Study NCT ID: NCT04875390
Status: COMPLETED
Last Update Posted: 2022-07-26
First Post: 2021-05-01

Brief Title: Erector Spina Plane ESP Block in Pediatric Patients
Sponsor: Ankara City Hospital Bilkent
Organization: Ankara City Hospital Bilkent

Study Overview

Official Title: Evaluation of the Effect of Ultrasonographic Guided Erector Spina Plan Block Application on Postoperative Analgesia in Infants Undergoing Laparotomy
Status: COMPLETED
Status Verified Date: 2022-07
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: In this study we aimed to evaluate the erector spina plane ESP block method that we used in our clinic with ultrasonography in pediatric cases between 1 month and 2 years of age who underwent laparotomy
Detailed Description: 36 patients who will undergo laparotomy between the ages of 1 month and 2 years in ASA American Society of Anesthesiologists I-II class will be included in the study patients will be divided into 2 groups Intraoperative erector spina plane block will be applied to the 1st group group E and intraoperative local anesthetic infiltration will be applied to the 2nd group group L Postoperative pain will be evaluated with the FLACC face legs activity crying consolation scale

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