Ignite Creation Date:
2024-05-06 @ 8:17 PM
Last Modification Date:
2024-10-26 @ 3:24 PM
Study NCT ID:
NCT06320743
Status:
ACTIVE_NOT_RECRUITING
Last Update Posted:
2024-03-21
First Post:
2024-03-12
Brief Title:
Cerebral and Peripheral Near Infrared Spectroscopy Monitoring in Low and High Flow Anaesthesia in Pediatric
Sponsor:
Ankara City Hospital Bilkent
Organization:
Ankara City Hospital Bilkent
Study Overview
Official Title:
Comparison of the Effects of Low and High Flow Sevoflurane Anesthesia on Cerebral and Peripheral Near Infrared Spectroscopy NIRS Values in Pediatric Patients
Status:
ACTIVE_NOT_RECRUITING
Status Verified Date:
2024-10
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:
To investigate the effects of non-invasive cerebral and peripheral NIRS monitoring and low and high flow sevoflurane anaesthesia on cerebral and peripheral NIRS in paediatric patients To determine the effects of two different flows on these monitoring techniques and thus to facilitate intraoperative patient monitoring and to predict complications hypoxia that may occur
Detailed Description:
The study will involve American Society of Anesthesiologists Physical Status Classification ASA I-III risk group patients aged between 2 and 12 years who will under go general anesthesia with a surgical procedure time of 1 hour or more and who will undergo pediatric surgery orthopedic and urological surgery will be included in the study Preoperative patients age gender height weight ASA score and operation type information will be recorded Patients will be randomized by the sealed envelope method and divided into 2 groups Low-Flow Anesthesia LFA and High-Flow Anesthesia HFA groups
Two groups will undergo NIRS monitoring alongside routine ASA monitoring Cerebral NIRS probe will be attached to the right and left frontotemporal region and a peripheral NIRS probe will be attached to the inner surface of the forearm and the basal values will be noted
Two groups will undergo NIRS monitoring alongside routine ASA monitoring Cerebral NIRS probe will be attached to the right and left frontotemporal region and a peripheral NIRS probe will be attached to the inner surface of the forearm and the basal values will be noted
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