Ignite Creation Date:
2024-05-06 @ 8:22 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06352606
Status:
RECRUITING
Last Update Posted:
2024-04-09
First Post:
2024-04-02
Brief Title:
Spinal and General Anesthesia in Neonates Undergoing Herniorrhaphy
Sponsor:
Tanta University
Organization:
Tanta University
Study Overview
Official Title:
Comparison Between Spinal and General Anesthesia in Neonates Undergoing Herniorrhaphy A Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-04
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:
The aim of this study is to compare spinal and general anesthesia in neonates undergoing herniorrhaphy
Detailed Description:
Spinal anesthesia SA is a fast simple and cost-effective method that has been used for the performance of inguinal hernias since the beginning of the 20th century in adults
One large observational study documented a low risk of post operative events with spinal anesthesia for inguinal hernia repair in infants In addition a randomized trial comparing reginal and general anesthesia in this population have not shown any significant differences in outcome Spinal anesthesia reduces postoperative oxygen desaturation and respiratory morbidity when compared to general anesthesia GA in infants who underwent inguinal herniorrhaphy
One large observational study documented a low risk of post operative events with spinal anesthesia for inguinal hernia repair in infants In addition a randomized trial comparing reginal and general anesthesia in this population have not shown any significant differences in outcome Spinal anesthesia reduces postoperative oxygen desaturation and respiratory morbidity when compared to general anesthesia GA in infants who underwent inguinal herniorrhaphy
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